Hydrochloric Acid → 2-Tert-butoxycarbonyloxyamino-4-methyl-thiazole-5-carboxylic acid

HRID 458235

반응식

HRID 458235 반응식
C([O:3][C:4]([C:6]1[S:10][C:9]([NH:11][O:12][C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])=[N:8][C:7]=1[CH3:20])=[O:5])C.[OH-].[K+].Cl>O1CCCC1CCO>[C:16]([O:15][C:13]([O:12][NH:11][C:9]1[S:10][C:6]([C:4]([OH:5])=[O:3])=[C:7]([CH3:20])[N:8]=1)=[O:14])([CH3:19])([CH3:17])[CH3:18]

참가 물질

5

반응 조건

온도
55 °C

실험 절차

A stirred solution of ethyl-2-tert-butoxycarbonyloxyamino-4-methyl-thiazole-5-carboxylate (10 g, 34.95 mmol) in tetrahydrofuran-ethanol (250 mL, 2:3) was treated with a 6N KOH solution (250 mL). The mixture was heated to 55° C. overnight. The solution was cooled to 0° C. and acidified with concd. HCl to pH 1. The solvent was evaporated in vacuo. The residue was washed with water, diethyl ether, dried in vacuo over anhydrous phosphorous pentoxide to obtain the title acid (6 g, 89%) as a white solid.

후처리

  1. temperatureThe solution was cooled to 0° C.
  2. customThe solvent was evaporated in vacuo
  3. washThe residue was washed with water, diethyl ether
  4. dry with materialdried in vacuo over anhydrous phosphorous pentoxide
  5. customto obtain the title acid (6 g, 89%) as a white solid

출처 및 근거

ORD 기록
ord-26345d7f07bf4078993b2a1d11025717
출처 데이터셋
uspto-grants-2007_03
특허 번호
US07189854B2

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