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Ethanol hydrochloride → HCID 66975073, 화합물

HRID 1022611
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인쇄 미리보기

반응식

HRID 1022611 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([C@@H:9]2[O:15][CH2:14][CH2:13][N:12](C(OC(C)(C)C)=O)[CH2:11][C@H:10]2[CH2:23][NH:24][C:25](=[O:29])[CH2:26][O:27][CH3:28])[CH:5]=[CH:6][C:7]=1[Cl:8].Cl.C(O)C>C(O)C>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]([C@@H:9]2[O:15][CH2:14][CH2:13][NH:12][CH2:11][C@H:10]2[CH2:23][NH:24][C:25](=[O:29])[CH2:26][O:27][CH3:28])[CH:5]=[CH:6][C:7]=1[Cl:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 21887872Ethanol hydrochlorideHCID 66975617HCID 66975617, 화합물

생성물 1

HCID 66975073HCID 66975073, 화합물수율 181%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of tert-butyl (6R,7R)-7-(3,4-dichlorophenyl)-6-{[(methoxyacetyl)amino]methyl}-1,4-oxazepane-4-carboxylate (161 mg) in ethanol (1 ml) was added 14.0 M hydrogen chloride-ethanol solution (2 mL), and the mixture was stirred at room temperature for 1 hr. The solvent was evaporated under reduced pressure. The obtained crystals were recrystallized from ethanol to give the title compound (125 mg) as colorless crystals.

후처리

  1. customThe solvent was evaporated under reduced pressure
  2. customThe obtained crystals were recrystallized from ethanol

출처 및 근거

ORD 기록
ord-7bf6a6a87c764d8fbe8691280a4c39c9
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08722662B2

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