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Hydrogen chloride-ethyl acetate → HCID 66975500, 화합물

HRID 1022683
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HRID 1022683 반응식
[C:1]([N:4]([CH2:6][C@H:7]1[C@H:13]([C:14]2[CH:19]=[CH:18][C:17]([Cl:20])=[C:16]([Cl:21])[CH:15]=2)[O:12][CH2:11][CH2:10][N:9](C(OC(C)(C)C)=O)[CH2:8]1)[CH3:5])(=[O:3])[CH3:2].C(OCC)(=O)C.Cl>>[ClH:20].[Cl:21][C:16]1[CH:15]=[C:14]([C@@H:13]2[O:12][CH2:11][CH2:10][NH:9][CH2:8][C@H:7]2[CH2:6][N:4]([CH3:5])[C:1](=[O:3])[CH3:2])[CH:19]=[CH:18][C:17]=1[Cl:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 21866389Hydrogen chloride-ethyl acetateHCID 66975244HCID 66975244, 화합물

생성물 1

HCID 66975500HCID 66975500, 화합물수율 140.8%

실험 절차

To tert-butyl (6R,7R)-6-{[acetyl(methyl)amino]methyl}-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate (100 mg) was added 4.0 M hydrogen chloride-ethyl acetate solution (4 mL), and the mixture was stirred at room temperature for 1 hr. The residue obtained by concentration under reduced pressure was separated by HPLC (C18, mobile phase: water/acetonitrile (containing 10 mM NH4HCO3)), and the obtained fraction was concentrated under reduced pressure to give the title compound (60 mg).

후처리

  1. customThe residue obtained by concentration under reduced pressure
  2. customwas separated by HPLC (C18, mobile phase: water/acetonitrile (containing 10 mM NH4HCO3))
  3. concentration
the obtained fraction was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-eb330e93e25d4de1982b5e5f7b9d55a9
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08722662B2

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