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2,6-Difluoro-4-prop-2-ynyloxy-benzylalcohol → (R)-2-Ethyl-piperazine-1,4-dicarboxylic acid 4-tert-butyl ester 1-(2,6-difluoro-4-prop-2-ynyloxy-benzyl)ester

HRID 1794145
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HRID 1794145 반응식
[F:1][C:2]1[CH:9]=[C:8]([O:10][CH2:11][C:12]#[CH:13])[CH:7]=[C:6]([F:14])[C:3]=1[CH2:4][OH:5].[C:15]([O:19][C:20]([N:22]1[CH2:27][CH2:26][N:25]([C:28](Cl)=[O:29])[C@H:24]([CH2:31][CH3:32])[CH2:23]1)=[O:21])([CH3:18])([CH3:17])[CH3:16]>>[F:1][C:2]1[CH:9]=[C:8]([O:10][CH2:11][C:12]#[CH:13])[CH:7]=[C:6]([F:14])[C:3]=1[CH2:4][O:5][C:28]([N:25]1[CH2:26][CH2:27][N:22]([C:20]([O:19][C:15]([CH3:17])([CH3:16])[CH3:18])=[O:21])[CH2:23][C@H:24]1[CH2:31][CH3:32])=[O:29]
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참가 물질

3

반응물 2

HCID 222199602,6-Difluoro-4-prop-2-ynyloxy-benzylalcoholHCID 86586001(R)-4-Chlorocarbonyl-3-ethyl-piperazine-1-carboxylic acid tert-butyl ester

생성물 1

HCID 86586002(R)-2-Ethyl-piperazine-1,4-dicarboxylic acid 4-tert-butyl ester 1-(2,6-difluoro-4-prop-2-ynyloxy-benzyl)ester수율 67%

실험 절차

This compound was prepared from 2,6-difluoro-4-prop-2-ynyloxy-benzylalcohol and (R)-4-chlorocarbonyl-3-ethyl-piperazine-1-carboxylic acid tert-butyl ester according to the procedure described in Example 179 to give the product as a colorless oil (336 mg; 67%); MS (ISP): 456.5 (M+NH4)+.

출처 및 근거

ORD 기록
ord-eeaeeb97c752497998243f7315b461fd
출처 데이터셋
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07022707B2

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