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Methyl 2-bromopropionate → HCID 16100377, 화합물

HRID 386515
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HRID 386515 반응식
[F:1][C:2]([F:16])([F:15])[C:3]1[CH:4]=[CH:5][C:6]([N:9]2[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]2)=[N:7][CH:8]=1.[CH3:17][O:18][C:19](=[O:23])[CH:20](Br)[CH3:21]>CO.CCN(C(C)C)C(C)C>[CH3:17][O:18][C:19](=[O:23])[CH:20]([N:12]1[CH2:11][CH2:10][N:9]([C:6]2[CH:5]=[CH:4][C:3]([C:2]([F:1])([F:15])[F:16])=[CH:8][N:7]=2)[CH2:14][CH2:13]1)[CH3:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 95576Methyl 2-bromopropionateHCID 6676181-(5-Trifluoromethyl-pyridin-2-yl)-piperazine

생성물 1

HCID 16100377HCID 16100377, 화합물

시약·촉매·용매 2

HCID 887Methanol용매HCID 81531Diisopropylethylamine용매

반응 조건

온도
70 °C

실험 절차

A solution of 1-(5-trifluoromethyl-pyridin-2-yl)-piperazine (0.9 g, 3.9 mmoles) in MeOH (13 mL) and DIPEA (1.5 mL) was treated with 2-bromo-propionic acid methyl ester (0.48 mL, 4.3 mmoles) and stirred overnight at 70° C. The MeOH was removed under reduced pressure and the residue was purified (silica gel, 10-40% acetone in hexane) to provide the title compound as a yellowish solid.

후처리

  1. customThe MeOH was removed under reduced pressure
  2. customthe residue was purified (silica gel, 10-40% acetone in hexane)

출처 및 근거

ORD 기록
ord-c3bb21b1bf6c4084ab82e6f2a536bec8
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08372841B2

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