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Hydrochloric Acid → 5-Bromo-3-((tert-butoxycarbonyl)amino)thiophene-2-carboxylic acid

HRID 532432
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HRID 532432 반응식
[OH-].[Li+].C[O:4][C:5]([C:7]1[S:8][C:9]([Br:20])=[CH:10][C:11]=1[NH:12][C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])=[O:6].Cl>C1COCC1.O>[Br:20][C:9]1[S:8][C:7]([C:5]([OH:6])=[O:4])=[C:11]([NH:12][C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 3939Lithium HydroxideHCID 57356848Methyl 5-bromo-3-((tert-butoxycarbonyl)amino)thiophene-2-carboxylate

생성물 1

HCID 219758545-Bromo-3-((tert-butoxycarbonyl)amino)thiophene-2-carboxylic acid

시약·촉매·용매 1

HCID 21881883Oxolane--water (1/1)용매

실험 절차

An aqueous 2 M lithium hydroxide solution (1 mL) was added to a solution of 5-bromo-3-tert-butoxycarbonylaminothiophene-2-carboxylic acid methyl ester (330.0 mg) in THF/water (1.6 mL/1.6 mL). The solution was stirred at room temperature overnight and was then neutralized with diluted HCl solution, and the solvent was removed in vacuo. The product with the molecular weight of 322.18 (C10H12BrNO4S) was obtained in this way; MS (ESI): 221, 223 (M-Boc+H+).

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후처리

  1. customthe solvent was removed in vacuo
  2. customThe product with the molecular weight of 322.18 (C10H12BrNO4S) was obtained in this way

출처 및 근거

ORD 기록
ord-4c14ad416ab34a00bac65c7b0205a07b
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08853208B2

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