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

HRID 1265627
ノート
印刷プレビュー

反応式

HRID 1265627 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
60 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-7877cd96d16d4d5b9c95c1b96a4aac7d
出典データセット
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06544985B2

反応ノート

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