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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 24985460, 화합물 → HCID 24985462, 화합물

HRID 913391
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HRID 913391 반응식
[Cl:1][C:2]1[C:10]([C:11]#[N:12])=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([CH2:18][OH:19])[N:6]2[CH2:13][C:14]([F:17])([F:16])[F:15]>CC#N.O=[Mn]=O>[Cl:1][C:2]1[C:10]([C:11]#[N:12])=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([CH:18]=[O:19])[N:6]2[CH2:13][C:14]([F:16])([F:17])[F:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 24985460HCID 24985460, 화합물

생성물 1

HCID 24985462HCID 24985462, 화합물수율 67%

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매2회HCID 6342Acetonitrile용매

실험 절차

To a solution of 4-chloro-2-(hydroxymethyl)-1-(2,2,2-trifluoroethyl)-1H-indole-5-carbonitrile (0.07 g, 0.24 mmol) in MeCN (3 mL) was added activated MnO2 (0.21 g, 2.42 mmol). The mixture was stirred at rt for 2 h. Additional MnO2 (0.11 g, 1.21 mmol) was added and stirred for 1 h. The solids were filtered off and washed with EtOAc, CH2Cl2 and MeOH. The filtrate was concentrated in vacuo and the residue was purified by radial chromatography (2-30% EtOAc-hexanes gradient) to afford the title compound (0.046 g, 67% yield): MS (ES) m/z 285 (M−1).

후처리

  1. stirringstirred for 1 h
  2. filtrationThe solids were filtered off
  3. washwashed with EtOAc, CH2Cl2 and MeOH
  4. concentrationThe filtrate was concentrated in vacuo
  5. customthe residue was purified by radial chromatography (2-30% EtOAc-hexanes gradient)

출처 및 근거

ORD 기록
ord-3867be54bc874a53ad7622c495754a93
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08026262B2

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