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Chemical Structure| 905300-50-7 Chemical Structure| 905300-50-7

Structure of 905300-50-7

Chemical Structure| 905300-50-7

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Product Details of [ 905300-50-7 ]

CAS No. :905300-50-7
Formula : C11H17BrN2O2S
M.W : 321.23
SMILES Code : O=C(OC(C)(C)C)N(C(C)C)C1=NC=C(Br)S1

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* 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 [ 905300-50-7 ]

[ 905300-50-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 67-63-0 ]
  • [ 405939-39-1 ]
  • [ 905300-50-7 ]
YieldReaction ConditionsOperation in experiment
90% With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; at 0 - 20℃; [00157] To a solution of tert-butyl 5 -bromothiazol-2-ylcarbamate (3 g, 10.7 mmol), isopropanol (6.40 g, 107.4 mmol) and triphenylphosphine (5.63 g, 21.5 mmol) in THF (30 mL) was added diethyl azodicarboxylate dropwise at O0C. The mixture was stirred at O0C and slowly warmed up to room temperature overnight. The solvent was evaporated. The residue was redissolved in dichloromethane (20 mL) and filtered to <n="55"/>get rid of the undissolved solid. The filtrate was concentrated and purified by column chromatography on silica gel using 100% hexane to give a light yellow oil (3.1O g, 90% yield). LCMS (Conditions C): 4.19 min (RT); (M+H)+ = 267.01 (100%), 265.01 (95%), 224.95 (60%), 222.95 (60%). 1H NMR, 400 MHz, CDCl3: delta 7.34 (s, 1 H), 5.29 (m, 1 H), 1.59 (s, 9 H), 1.45 (d, 6.8 Hz, 6 H).
90% With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; at 0 - 20℃; To a solution of tert-butyl 5 -bromothiazol-2-ylcarbamate (3 g, 10.7 mmol), isopropanol (6.40 g, 107.4 mmol) and triphenylphosphine (5.63 g, 21.5 mmol) in THF (30 mL) was added diethyl azodicarboxylate dropwise at O0C. The mixture was stirred at O0C and slowly warmed up to room temperature overnight. The solvent was evaporated. The residue was redissolved in dichloromethane (20 mL) and filtered to <n="65"/>get rid of the undissolved solid. The filtrate was concentrated and purified by column chromatography on silica gel using 100% hexane to give a light yellow oil (3.1O g, 90% yield). LCMS (Conditions C): 4.19 min (RT); (M+H)+ = 267.01 (100%), 265.01 (95%), 224.95 (60%), 222.95 (60%). 1H NMR, 400 MHz, CDCl3: delta 7.34 (s, 1 H), 5.29 (m, 1 H), 1.59 (s, 9 H), 1.45 (d, 6.8 Hz, 6 H).
79% Step 2: Preparation 18b; To a solution of Preparation 18a (10 g, 36 mmol), triphenylphosphine (14.1 g, 54 mmol), and isopropanol (4.1 mL, 54 mmol) in THF (75 mL) at rt was slowly added diethyl azodicarboxylate (8.4 mL, 54 mmol) over 10 min causing a slight exothermic reaction. After stirring for 2.5 h at rt, the reaction was concentrated in vacuo to remove the THF and the remaining material was dissolved in ethyl acetate (150 mL). The solution was washed with 1 N aq. HCl (3×100 mL), water (50 mL), and satd. Aq. sodium bicarbonate (50 mL), then dried over anhyd sodium sulfate, filtered, and concentrated in vacuo to afford a thick reddish-brown oil. Approximately 50 mL of ethyl acetate was added causing a precipitate to form from the solution. The solution was filtered to remove the solid and the resulting clear solution was concentrated. To the resulting material was then added diethyl ether (200 mL) and a 20% aq. solution of Oxone was added and the mixture was stirred vigorously at rt for ?16 h. Ethyl acetate (200 mL) was added and the resulting layers were separated. The organic layer was concentrated and the resulting oil was purified by flash chromatography on silica gel using a gradient elution from 5% to 10% ethyl acetate in hexanes as the eluant. Fractions containing the product were collected and concentrated to afford 9.2 g (79%) of a grey solid as Preparation 18b. HPLC Ret. time: 4.20 min.
5.0 g With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 - 75℃; for 3.16667h;Inert atmosphere; A mixture of <strong>[405939-39-1]tert-butyl (5-bromothiazol-2-yl)carbamate</strong> (5.0g, 18.0 mmol), PPh3 (10.37 g, 39.57 mmol) and IPA (3.2 g, 54.0 mmol) in THF (50 ml) was cooled at 0C under N2 atmosphere. DIAD (7.70 ml, 39.6 mmol) was added dropwise to the reaction mixture at 0C. The reaction mixture was stirred at rt for 10 min and then heated to 75 C for 3 h. The resulting reaction mixture cooled to rt and was concentrated under reduced pressure. The residue was purified by column chromatography (2-5% EtOAc in hexane) yielding tert-butyl (5-bromothiazol-2-yl)(isopropyl)carbamate (5.0 g, 15.62 mmol). LCMS: Method C, 3.11 min, MS: ES+ 321.1, 323.1(M + 2); NMR (400 MHz, CDC13) delta ppm 7.36 (s, 1, 1H), 5.26 - 5.33 (m, 1H), 1.61 (s, 9H), 1.45 (d, J=7.2 Hz, 6H).

 

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