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HCID 86632366, 화합물 → HCID 86632367, 화합물

HRID 2428147
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HRID 2428147 반응식
[C:1]([O:5][C:6](=[O:23])[N:7]([CH2:12][CH2:13][C:14]1[CH:19]=[CH:18][C:17]([Cl:20])=[C:16]([CH2:21][OH:22])[CH:15]=1)[CH2:8][CH:9]([F:11])[F:10])([CH3:4])([CH3:3])[CH3:2]>CC#N.O=[Mn]=O>[C:1]([O:5][C:6](=[O:23])[N:7]([CH2:12][CH2:13][C:14]1[CH:19]=[CH:18][C:17]([Cl:20])=[C:16]([CH:21]=[O:22])[CH:15]=1)[CH2:8][CH:9]([F:11])[F:10])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 86632366HCID 86632366, 화합물

생성물 1

HCID 86632367HCID 86632367, 화합물수율 94%

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매HCID 6342Acetonitrile용매

실험 절차

MnO2 (6.35 g, 65.7 mmol) was added to a sol. of [2-(4-chloro-3-hydroxymethyl-phenyl)-ethyl]-(2,2-difluoro-ethyl)-carbamic acid tert-butyl ester (4.60 g, 13.2 mmol) in CH3CN (133 mL). The mixture was stirred at rt for 4 h. The mixture was filtered over celite, and the precipitate was washed with CH3CN and CH2Cl2. The filtrate was evaporated under reduced pressure to yield to crude title compound (4.30 g, 94%) that was used further without purification. LC-MS: tR=1.06 min.

후처리

  1. filtrationThe mixture was filtered over celite
  2. washthe precipitate was washed with CH3CN and CH2Cl2
  3. customThe filtrate was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-872bed40de9945f7be3d42ae4c48c107
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07968720B2

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