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Chemical Structure| 1349902-20-0 Chemical Structure| 1349902-20-0

Structure of 1349902-20-0

Chemical Structure| 1349902-20-0

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Product Details of [ 1349902-20-0 ]

CAS No. :1349902-20-0
Formula : C9H10N2O3S
M.W : 226.25
SMILES Code : O=C(C1=C2CCC1)NC(N2CC(O)=O)=S
MDL No. :MFCD28405597

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Application In Synthesis of [ 1349902-20-0 ]

* 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 [ 1349902-20-0 ]

[ 1349902-20-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1349902-20-0 ]
  • [ 352-11-4 ]
  • [ 356058-42-9 ]
YieldReaction ConditionsOperation in experiment
97% Example 7 - Alternative method for making (2-[(4-Fluorophenyl)methyl]thio}-4-oxo-4,5,6,7- tetrahydro-lHcyclopenta[d]pyrimidin-l-yl)acetic acid) (4-Oxo-2-thioxo-2,3,4,5,6,7-hexahydro-lH- cyclopenta [ /]pyrimidin-l-yl)acetic acid (20.0 g, 1.0 eq) was slurried in a mixture of water (112 mL) and isopropyl alcohol (20 mL). NaOH solution (50.9% aqueous, 13.82 g, 1.99 eq) was added followed by a water line wash (10 mL) resulting in a solution. Then Na2C03 (1.50 g, 0.16 eq) was charged and the solution was heated to 40+/-3 C. Thereafter 4-fluorobenzyl chloride (13.4 g, 1.05 eq) was added, followed by a line wash of isopropyl alcohol (12 mL) and the reaction mixture was stirred at 40+/-3 C until the reaction was deemed complete ( ~2.5 hours). The reaction mixture was cooled to 20+/-3 C and formic acid (2.4 g, 0.6 eq) was added resulting in crystallisation of the product within 30 minutes. A second charge of formic acid (6.9 g, 1.7 eq) was added over 1 hour and the slurry was stirred at 20+/-3 C for at least one hour. The slurry was filtered to isolate the product, which was washed twice with a mixture of water (32 mL) and isopropyl alcohol (8 mL), then with isopropyl alcohol (40 mL) and dried in vacuo at 50 C to yield the title compound as an off-white solid (28.6 g, 97%th). 1H NM R (d6 DMSO) delta 1.95 (2H, m), 2.57 (2H, t), 2.85 (2H, t), 4.4 (2H, s), 4.7 (2H, s), 7.15 (2H, dd), 7.45 (2H, dd), ~13.6 (1H, vbrs).
76% With potassium carbonate; potassium hydroxide; In water; isopropyl alcohol; at 40℃; for 3h; Compound 1 (0.3603 g, 1.6 mmol, 1 eq) was stirred in a mixture of water (2 mL) and isopropyl alcohol (360 muL). KOH aqueous solution (50% w/v, 500 muL, 1.9 eq) was added. K2CO3 (0.0332 g, 0.24 mmol, 0.15 eq) was added and the solution was heated to 40 C. Then 4-fluorobenzyl chloride (0.2197 g, 1.52 mmol, 0.95 eq) was added and the reaction was stirred at 40 C for 3 hours. The reaction was cooled to room temperature and formic acid (30 muL, 0.8 mmol, 0.5 eq) was added to crystallize the product. After 30 min, more formic acid (103 muL, 2.7 mmol, 1.7 eq) was slowly added and the reaction was stirred for at least an hour until crystallization was complete. The product was isolated through filtration and washed twice with a 4:1 mixture of water and isopropyl alcohol (1 mL), then with isopropyl alcohol (1 mL). The product was stirred in ether for 2 hours to remove remaining organic impurities and filtered again. Product was dried in vacuo at 50 C to yield 2 (0.4082g, 1.22 mmol, 76%).
60% With potassium carbonate; potassium hydroxide; In Isopropyl acetate; water; at 40℃; for 3h; Compound 1 (1 eq, 1.62 mmol) was stirred in a mixture of water (3 mL) and isopropyl alcohol (820 muL). KOH aqueous solution (50% w/v, 1.9 eq, 3.08 mmol) was added followed by K2CO3 (0.15 eq, 0.24 mmol) and the reaction was heated to 40 C under stirring. 4-fluorobenzyl chloride (0.95 eq, 1.52 mmol) was then added and the reaction was stirred at 40 C for 3 hours. The reaction was cooled to room temperature and formic acid (0.5 eq, 0.8 mmol) was added to crystallize the product. After 1h, more formic acid (1.7 eq, 2.7 mmol) was slowly added and the reaction was stirred for an hour until crystallization was complete. The product was collected through filtration and washed twice with a 4:1 (v:v) mixture of water and isopropyl alcohol (1 mL) followed by isopropyl alcohol (1 mL). The product was stirred in ether overnight and filtered again. Product was dried at 50 C to obtain the title compound as a colourless solid (300 mg, 60%). 1H NMR (DMSO-d6) delta: 12.54 (s, 1H), 7.47 (m, 2H), 7.11 (m, 2H), 4.65 (s, 2H), 4.45 (s, 2H), 2.82 (t, J = 7.3 Hz, 2H), 2.60 (t, J = 7.3 Hz, 2H), 1.99 (quint, J = 7.3 Hz, 2H).
60% With potassium carbonate; potassium hydroxide; In water; isopropyl alcohol; at 40℃; for 3h; Compound 11' (1 eq, 1.62 mmol) was stirred in a mixture of water (3 mL) and isopropyl alcohol (820 mu). KOH aqueous solution (50% w/v, 1.9 eq, 3.08 mmol) was added followed by K2CO3 (0.15 eq, 0.24 mmol) and the reaction was heated to 40C under constant stirring. 4-fluorobenzyl chloride (0.95 eq, 1.52 mmol) was then added and the reaction was stirred at 40C for 3 hours. The reaction was cooled to room temperature and formic acid (0.5 eq, 0.8 mmol) was added to crystallize the product. After lh, more formic acid (1.7 eq, 2.7 mmol) was slowly added and the reaction was stirred for at least an hour until crystallization was complete. The product was collected through filtration and washed twice with a 4: 1 (v:v) mixture of water and isopropyl alcohol (1 mL) followed by isopropyl alcohol (1 mL). The product was stirred in ether overnight to remove remaining organic impurities and filtered again. Product was dried at 50C to afford the title compound as a colourless solid (300 mg, 60%). M.p. 183-185C 1H-NMR (CDCI3, 600 MHz) delta 12.54 (s, 1H), 7.45 (dd, J = 8.6, 5.6, 2H), 7.11 (t, J = 8.6, 2H), 4.63 (s, 2H), 4.43 (s, 2H), 2.82 (t, J = 7.3, 2H), 2.59 (t, J = 7.3, 2H), 1.97 (q, J = 1.3, 2H); 13C-NMR (CDCI3, 150 MHz) delta: 168.3, 165.7, 161.6 (d, JCF = 240 Hz), 156.7, 133.2 (d, JCF = 3 Hz), 131.3 (d, JCF = 7.5 Hz), 119.8, 115.3 (d, JCf = 21Hz), 50.1, 34.6, 31.4, 28.0, 20.2 ;

 

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