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2-Amino-2-thioxoethyl 2,2-dimethylpropanoate → Methyl 3-[2-hydroxymethyl-5-methyl-thiazol-4-yl]-benzoate

HRID 1265627
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HRID 1265627 반응식
[CH3:1][O:2][C:3](=[O:17])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10](=O)[CH:11](Br)[CH2:12]CC)[CH:5]=1.C(C([O:24][CH2:25][C:26]([NH2:28])=[S:27])=O)(C)(C)C>CCO>[CH3:1][O:2][C:3](=[O:17])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]2[N:28]=[C:26]([CH2:25][OH:24])[S:27][C:11]=2[CH3:12])[CH:5]=1
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4

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HCID 27821132-Amino-2-thioxoethyl 2,2-dimethylpropanoateHCID 87951238Rac-3-(2-bromo-pentanoyl)-benzoic acid methyl ester

생성물 1

HCID 18548740Methyl 3-[2-hydroxymethyl-5-methyl-thiazol-4-yl]-benzoate수율 83.3%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
60 °C

실험 절차

A sample of rac-3-(2-bromo-pentanoyl)-benzoic acid methyl ester (0.60 g) and and 2-(tert.-butylcarbonyloxy)thioacetamide (0.36 g) in EtOH (4 mL) was heated at reflux for 5 h. The mixture was partitioned between AcOEt and 5% NaHCO3 solution, the organic layer was washed with brine, dried and evaporated. A solution of the residual oil and of NaOMe (0.13 g) in MeOH (10 mL) was stirred at 60° C. for 30 min. The solution was diluted with AcOEt, washed with 1N HCl and brine, dried and evaporated to give 3-(2-hydroxymethyl-5-methyl-thiazol-4-yl)-benzoic acid methyl ester (0.44 g) as an oil.

후처리

  1. temperatureat reflux for 5 h
  2. customThe mixture was partitioned between AcOEt and 5% NaHCO3 solution
  3. washthe organic layer was washed with brine
  4. customdried
  5. customevaporated
  6. additionThe solution was diluted with AcOEt
  7. washwashed with 1N HCl and brine
  8. customdried
  9. customevaporated

출처 및 근거

ORD 기록
ord-7877cd96d16d4d5b9c95c1b96a4aac7d
출처 데이터셋
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06544985B2

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