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Chemical Structure| 1206824-76-1 Chemical Structure| 1206824-76-1

Structure of 1206824-76-1

Chemical Structure| 1206824-76-1

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Product Details of [ 1206824-76-1 ]

CAS No. :1206824-76-1
Formula : C10H15N3O3
M.W : 225.24
SMILES Code : O=C(OC(C)(C)C)NN1C(C(N)=O)=CC=C1
MDL No. :MFCD24471141

Safety of [ 1206824-76-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 1206824-76-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1206824-76-1 ]

[ 1206824-76-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 937046-96-3 ]
  • [ 1206824-76-1 ]
YieldReaction ConditionsOperation in experiment
73.6% With ammonium hydroxide; dihydrogen peroxide; In ethanol; water; at 20℃; h. To a stirred solution of tert-butyl 2-cyano-lH-pyrrol-l-ylcarbamate 13 (5g, 24.12 mmol) in ethyl alcohol (100 ml) was added concentrated aqueous ammonium hydroxide solution (50 mL) at 20 0C followed by hydrogen peroxide (7.4 mL, 72.38 mmol, 30 % in water) slowly at 20 0C and stirred at the same temperature for 16 h. Reaction mixture was concentrated in vacuum and diluted with ethyl acetate (150 mL), washed with water ( 2 x 50 mL). The aqueous layer was extracted with ethyl acetate (150 mL). The combined ethyl acetate layers were washed with water (100 mL), brine (50 mL), dried, filtered, and concentrated in vacuum. The residue obtained was crystallized from diisopropyl ether and hexane to afford tert-butyl 2-carbamoyl-lH-pyrrol-l-ylcarbamate 14 (4.0 g, 73.6%) as a colorless solid. 1H NMR (300 MHz, DMSO) delta 9.89 (s, IH, D2O exchangeable), 7.31 (d, J= 38.5, IH), 6.84 (dd, J= 1.9, 2.8, 2H, IH is D2O exchangeable), 6.76 (dd, J= 1.9, 4.2, IH), 5.97 (dd, J= 2.8, 4.2, IH), 1.40 (s, 9H). HPLC (Zorbax SBC3, 3.0 x 150 mm, 5 mum, with ZGC SBC3, 2.1 x 12.5 mm guard cartridge. Mobile phase: 0.1 M ammonium acetate/ Acetonitrile) Rt = 12.817, (97.6861 %). Analysis: CaIC fOr C10H15N3O3: C, 53.32; H, 6.71; N, 18.65 Found: C, 53.40; H, 6.74; N, 18.55.
73.6% With ammonium hydroxide; dihydrogen peroxide; In ethanol; water; at 20℃; for 16h; To a stirred solution of tert-butyl 2-cyano-lH-pyrrol-l-yl carbamate 12d (5g, 24.12 mmol) in ethyl alcohol (100 ml) was added concentrated aqueous ammonium hydroxide solution (50 mL) at 20 C followed by hydrogen peroxide (7.4 mL, 72.38 mmol, 30 % in water) slowly at 20 C and stirred at the same temperature for 16 h. Reaction mixture was concentrated in vacuum and diluted with ethyl acetate (150 mL), washed with water ( 2 x 50 mL). The aqueous layer was extracted with ethyl acetate (150 mL). The combined ethyl acetate layers were washed with water (100 mL), brine (50 mL), dried, filtered, and concentrated in vacuum. The residue obtained was crystallized from diisopropyl ether and hexane to afford tert-butyl 2-carbamoyl- lH-pyrrol-l-ylcarbamate 12e (4.0 g, 73.6%) as a colorless solid. 1H NMR (300 MHz, DMSO) delta 9.89 (s, 1H, D20 exchangeable), 7.31 (d, J= 38.5, 1H), 6.84 (dd, J= 1.9, 2.8, 2H, 1H is D20 exchangeable), 6.76 (dd, J= 1.9, 4.2, 1H), 5.97 (dd, J= 2.8, 4.2, 1H), 1.40 (s, 9H). HPLC (Zorbax SBC3, 3.0 x 150 mm, 5 mu?iota, with ZGC SBC3, 2.1 x 12.5 mm guard cartridge. Mobile phase: 0.1 M ammonium acetate/ Acetonitrile) Rt = 12.817, (97.6861 %). Analysis: Calc for C10H15N3O3: C, 53.32; H, 6.71 ; N, 18.65 Found: C, 53.40; H, 6.74; N, 18.55.
73.6% With ammonium hydroxide; water; dihydrogen peroxide; In ethanol; at 20℃; for 16h; Step 1:To a stirred solution of tert-butyl hydrazinecarboxylate 22b (50 g, 412.37 mmol) and 2,5-dimethoxytetrahydrofuran 22a (54.5 g, 412.37 mmol) in dioxane (300 mL) was added aqueous hydrochloric acid (5 mL, 2N). The reaction was set up using a dean-stark apparatus and heated at 90 C for 20 h. Reaction mixture was cooled to 20 C, neutralized with saturated sodium bicarbonate (18 mL) and filtered to remove inorganics. The filtrate was concentrated in vacuum and triturated with ether. The solid obtained was collected by filtration to furnish on drying tert-butyl lH-pyrrol-l-ylcarbamate 22c (43 g, 57.2%) as a yellow brown solid. 1H NMR (300 MHz, CD3OD) ? 6.62 (t, J= 2.3, 2H), 6.02 (t, J= 2.3, 2H), 1.48 (s, 9H); MS (ES+): 181.1 (M _1). Analysis: Calculated for C9Hi4N202: C, 59.32; H, 7.74; N, 15.37. Found: C, 59.32; H, 7.65; N, 15.02. Step 2:To a stirred solution of tert-butyl lH-pyrrol-l-ylcarbamate 22c (40 g, 219.52 mmol), in acetonitrile (350 mL) was added chlorosulfonyl isocyanate (32.62 g, 230.50 mmol) slowly at 0 C and continued stirring at 0 C for 30 min. To the solution N, N-dimethyl formamide (40 mL) was added below 5 C and continued stirring at 0 C for 1 hr. The reaction mixture was poured into a mixture of crushed ice (1 L) and ethyl acetate (1 L). The layers were separated and the organic layer was washed with water (500 mL), brine (250 mL), dried and concentrated in vacuum to furnish crude (43 g) product. The crude was purified by flash chromatography (silica gel, eluting with ethyl acetate in hexane0-50%) to afford pure tert-butyl 2-cyano-lH-pyrrol-l-ylcarbamate 22d (30 g, 66 %>) as a colorless solid. 1H NMR (300 MHz, DMSO-d6) ? 10.80 (s, 1H, D20 exchangeable), 7.23 (dd, J= 1.7, 2.9, 1H), 6.94 (dd, J= 1.7, 4.3, 1H), 6.20 (dd, J= 2.9, 4.3, 1H), 1.45 (s, 9H). Analysis: Calculated for Ci0Hi3N3O2: C, 57.95; H, 6.32; N, 20.27. Found: C, 58.02; H, 6.45; N, 20.18. Step 3:To a stirred solution of tert-butyl 2-cyano-lH-pyrrol-l-ylcarbamate 22d (5 g, 24.12 mmol) in ethyl alcohol (100 mL) was added concentrated aqueous ammonium hydroxide solution (50 mL) at 20 C followed by hydrogen peroxide (7.4 mL, 72.38 mmol, 30 % in water) slowly at 20 C and stirred at the same temperature for 16 h. Reaction mixture was concentrated in vacuum and diluted with ethyl acetate (150 mL), washed with water (2 x 50 mL). The aqueous layer was extracted with ethyl acetate (150 mL). The combined ethyl acetate layers were washed with water (100 mL), brine (50 mL), dried, filtered, and concentrated in vacuum. The residue obtained was crystallized from diisopropyl ether and hexane to afford tert-butyl 2-carbamoyl-lH-pyrrol-l-ylcarbamate 22e (4.0 g, 73.6%) as a colorless solid. 1H NMR (300 MHz, DMSO-d6) ? 9.89 (s, 1H, D20 exchangeable), 7.31 (d, J = 38.5, 1H), 6.84 (dd, J= 1.9, 2.8, 2H, lH is D20 exchangeable), 6.76 (dd, J = 1.9, 4.2, 1H), 5.97 (dd, J= 2.8, 4.2, 1H), 1.40 (s, 9H); Analysis: Calculated for Ci0Hi5N3O3: C, 53.32; H, 6.71 ; N, 18.65. Found: C, 53.40; H, 6.74; N, 18.55. Step 4:To a solution of tert-butyl 2-carbamoyl-lH-pyrrol-l-ylcarbamate 22e (2g, 8.87 mmol) in dichloromethane (15 mL) was added trifluoro acetic acid (15 mL) at 20 C and stirred for 30 min. The reaction mixture was concentrated to dryness to remove excess trifluoroacetic acid and diluted with dichloromethane. Triethylorthoformate (30 mL) was added to the residue and was heated to 79 C overnight. Reaction mixture was concentrated to dryness and triturated with hexanes, the solid obtained was collected by filtration dried in vacuum to give crude pyrrolo[l ,2-f][l ,2,4]triazin-4-ol 22f (1.1 g, 91%) as a dark brown solid. 1H NMR (300 MHz, DMSO-d6) ? 11.63 (s, 1H, D20 exchangeable), 7.83 (d, J= 4.0, 1H), 7.59 (dd, J= 1.7, 2.6, 1H), 6.89 (dd, J= 1.6, 4.3, 1H), 6.54 (dd, J = 2.7, 4.3, 1H); MS (ES+): 136.2 (M + l). Step 5:The stirred solution of pyrrolo[l ,2-f][l ,2,4]triazin-4-ol 22f (1 g, 7.40 mmol), benzyltriethylammonium chloride (3.29 g, 14.80 mmol), and N,N-dimethylaniline (1.35 g, 1 1.10 mmol) in acetonitrile (25 mL) was heated to 80 C and at this temperature phosphorous oxy chloride (6.88 g, 44.40 mmol) was added and stirred at 80 C for 16 h. The reaction was concentrated to remove acetonitrile and phosphorus oxy chloride. The reaction was quenched by adding ice water (20 mL) and extracted with ethyl acetate (2 x 100 mL). The ethyl acetate extracts were combined washed with hydrochloric acid (1 N, 30 mL), water (50 mL), saturated sodium bicarbonate (1 x 20 mL), water (50 mL), brine (20 mL) dried and concentrated. The crude residue was purified by flash chromatography (silica gel, eluting with ethyl acetate in hexanes (0 to 5 %)) to furnish pure4-chloropyrrolo[l,2-fJ[l,2,4]triazine 22g (0.7 g, 61.6 %) as a colorless oil, which solidified on standing in refrigerator. 1H NMR (300 MHz, DMSO-d6) ? 8.44 (s, 1H), 8.27 (dd, J = 1.5, 2.5, 1H), 7.12 (qd, J= 2.0, 4.6, 2H). Step 6:A solution of 2-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)aniline (10m) (2.3 g, 9.8 ...
 

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