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Trifluoroacetic acid → 5-carboxymethoxy-3-(1-naphthoyl)-N-pentyl-1H-indole

HRID 55928
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인쇄 미리보기

반응식

HRID 55928 반응식
[OH:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH2:11][CH2:12][CH2:13][CH2:14][CH3:15])[CH:6]=[C:5]2[C:16]([C:18]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH:21]=[CH:20][CH:19]=1)=[O:17].[C:28]([OH:34])([C:30](F)(F)F)=[O:29]>ClCCl>[C:28]([CH2:30][O:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH2:11][CH2:12][CH2:13][CH2:14][CH3:15])[CH:6]=[C:5]2[C:16]([C:18]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH:21]=[CH:20][CH:19]=1)=[O:17])([OH:34])=[O:29]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 53394447JWH 018 5-hydroxyindole metabolite

생성물 1

HCID 681593415-carboxymethoxy-3-(1-naphthoyl)-N-pentyl-1H-indole

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 7 (3.0 g, 6 4 mmol) in dichloromethane (50 ml) was added TFA (25 ml) and the mixture was stirred at room temperature for 3 h. The mixture was evaporated to dryness and the crude obtained was purified by chromatography on silica-gel using 5% methanol in chloroform to give Hapten-B (2.1 g, 79%).

후처리

  1. customThe mixture was evaporated to dryness
  2. customthe crude obtained
  3. customwas purified by chromatography on silica-gel
  4. customto give Hapten-B (2.1 g, 79%)

출처 및 근거

ORD 기록
ord-7d99fefe344d435782ca7a1b917eab47
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09434687B2

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