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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrogen Bromide → 3-Amino-2-hydroxy-4-(2-thienyl)butanamide

HRID 12435
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HRID 12435 반응식
Br.[NH2:2][C:3](=[O:24])[CH:4]([OH:23])[CH:5]([NH:12]C(=O)OCC1C=CC=CC=1)[CH2:6][C:7]1[S:8][CH:9]=[CH:10][CH:11]=1>C(O)(=O)C>[NH2:12][CH:5]([CH2:6][C:7]1[S:8][CH:9]=[CH:10][CH:11]=1)[CH:4]([OH:23])[C:3]([NH2:2])=[O:24]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 260Hydrogen BromideHCID 86623368HCID 86623368, 화합물

생성물 1

HCID 667184663-Amino-2-hydroxy-4-(2-thienyl)butanamide수율 131.3%

시약·촉매·용매 1

HCID 176Acetic Acid용매2회

실험 절차

70 ml of 30% HBr in glacial acetic acid were added to 11 g of phenylmethyl [3-amino-2-hydroxy-3-oxo-1-(2-thienylmethyl)propyl]carbamate (29.66 mmol) in 30 ml of glacial acetic acid. After about 2 hours, the mixture was concentrated and the resulting residue was stirred firstly with cyclohexane and then with dichloromethane. 7.8 g of the title compound were obtained as hydrobromide.

후처리

  1. concentrationthe mixture was concentrated

출처 및 근거

ORD 기록
ord-4c437eb2a50340bdb7d8605ab5fe4e4d
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07728012B2

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