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

HRID 1266771
ノート
印刷プレビュー

反応式

HRID 1266771 の反応式
Br[CH:2]([CH3:15])[C:3]([C:5]1[CH:6]=[C:7]([CH:12]=[CH:13][CH:14]=1)[C:8]([O:10][CH3:11])=[O:9])=O.C(C([O:22][CH2:23][C:24]([NH2:26])=[S:25])=O)(C)(C)C>CCO>[OH:22][CH2:23][C:24]1[S:25][C:2]([CH3:15])=[C:3]([C:5]2[CH:6]=[C:7]([CH:12]=[CH:13][CH:14]=2)[C:8]([O:10][CH3:11])=[O:9])[N:26]=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 22139798Rac-3-(2-bromo-propionyl)-benzoic acid methyl ester

生成物 1

HCID 18548740Methyl 3-[2-hydroxymethyl-5-methyl-thiazol-4-yl]-benzoate収率 44.6%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
60 °C

実験手順

A solution of methyl 3-(2-bromo-propionyl)-benzoate (2.7 g) and 2-(tert.-butyl-carbonyloxy)thioacetamide (2.1 g) in EtOH (20 mL) was heated at reflux for 8 h. The mixture was partitioned between H2O and AcOEt. The organic layer was dried and evaporated. The residue was dissolved in MeOH (20 ml), NaOMe (0.54 g) was added, and the mixture was heated to 60° C. for 1 h. The mixture was diluted with AcOEt and then washed with 3N HCl and brine. The organic layer was dried and evaporated and the residue was crystallized from AcOEt to give methyl 3-[2-hydroxymethyl-5-methyl-thiazol-4-yl]-benzoate (1.17 g) as white solid.

後処理

  1. temperatureat reflux for 8 h
  2. customThe mixture was partitioned between H2O and AcOEt
  3. customThe organic layer was dried
  4. customevaporated
  5. dissolutionThe residue was dissolved in MeOH (20 ml)
  6. additionNaOMe (0.54 g) was added
  7. additionThe mixture was diluted with AcOEt
  8. washwashed with 3N HCl and brine
  9. customThe organic layer was dried
  10. customevaporated
  11. customthe residue was crystallized from AcOEt

出典と根拠

ORDレコード
ord-780c0c6dc70f4ae28f07998a4264b8ef
出典データセット
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06548495B2

反応ノート

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