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

HRID 1266771
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HRID 1266771 반응식
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
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참가 물질

4

반응물 2

HCID 27821132-Amino-2-thioxoethyl 2,2-dimethylpropanoateHCID 22139798Rac-3-(2-bromo-propionyl)-benzoic acid methyl ester

생성물 1

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

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
60 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-780c0c6dc70f4ae28f07998a4264b8ef
출처 데이터셋
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06548495B2

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