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Dichloromethane → 3-(4-Methylpiperazin-1-yl)benzoic acid

HRID 1058581
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인쇄 미리보기

반응식

HRID 1058581 반응식
C([O:5][C:6](=[O:20])[C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([N:13]2[CH2:18][CH2:17][N:16]([CH3:19])[CH2:15][CH2:14]2)[CH:8]=1)(C)(C)C.C(Cl)Cl>C(O)(C(F)(F)F)=O.C1(C)C=CC=CC=1>[CH3:19][N:16]1[CH2:15][CH2:14][N:13]([C:9]2[CH:8]=[C:7]([CH:12]=[CH:11][CH:10]=2)[C:6]([OH:20])=[O:5])[CH2:18][CH2:17]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6344DichloromethaneHCID 543335303-(4-Methylpiperazinyl)-benzoic acid tert-butyl ester

생성물 1

HCID 47416813-(4-Methylpiperazin-1-yl)benzoic acid

시약·촉매·용매 2

HCID 1140Toluene용매HCID 6422Trifluoroacetic acid용매

실험 절차

3-(4-Methylpiperazinyl)-benzoic acid tert-butyl ester (4.1 g, 14.9 mmol) was dissolved in TFA: CH2Cl2 (70 ml, 1:1) and the reaction was stirred for 2 h at RT. The reaction mixture was diluted with toluene (100 ml), then was concentrated in vacuo and was used in the next reaction without further purification: MS (ES+) 221.3 (M+H+).

후처리

  1. concentrationwas concentrated in vacuo
  2. customwas used in the next reaction without further purification

출처 및 근거

ORD 기록
ord-d3109afe8a8a4b86b0ce03a452ab6b4a
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06518267B1

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