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Trifluoroacetic acid → [4-(2-Aminoethyl)-1-piperazinyl](3,4-dichlorophenyl)methanone trifluoroacetate

HRID 496880
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인쇄 미리보기

반응식

HRID 496880 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:23]=[CH:24][C:25]=1[Cl:26])[C:5]([N:7]1[CH2:12][CH2:11][N:10]([CH2:13][CH2:14][NH:15]C(=O)OC(C)(C)C)[CH2:9][CH2:8]1)=[O:6].[F:27][C:28]([F:33])([F:32])[C:29]([OH:31])=[O:30]>ClCCl>[F:27][C:28]([F:33])([F:32])[C:29]([OH:31])=[O:30].[NH2:15][CH2:14][CH2:13][N:10]1[CH2:11][CH2:12][N:7]([C:5]([C:4]2[CH:23]=[CH:24][C:25]([Cl:26])=[C:2]([Cl:1])[CH:3]=2)=[O:6])[CH2:8][CH2:9]1
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 22322333tert-Butyl 2-[4-(3,4-dichlorobenzoyl)-1-piperazinyl]ethylcarbamate

생성물 1

HCID 22322358[4-(2-Aminoethyl)-1-piperazinyl](3,4-dichlorophenyl)methanone trifluoroacetate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

The product from step (ii) above (3.3 g) was dissolved in dichloromethane (50 ml) and trifluoroacetic acid (10 ml) added. After 16 hours at room temperature the solvent was removed to give the sub-titled product as an oil (5.9 g).

후처리

  1. customAfter 16 hours at room temperature the solvent was removed

출처 및 근거

ORD 기록
ord-1591b1d4ccf24aebb60c8cb4113c009f
출처 데이터셋
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06946478B2

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