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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(2S)-2-Ethyl-4-(phenylmethyl)-1-piperazinecarboxylic acid, 1,1-dimethylethyl ester → (S)-2-Ethylpiperazine, N1-BOC protected

HRID 38277
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인쇄 미리보기

반응식

HRID 38277 반응식
[CH2:1]([C@H:3]1[CH2:8][N:7](CC2C=CC=CC=2)[CH2:6][CH2:5][N:4]1[C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17])[CH3:2]>CCO.[Pd]>[CH2:1]([C@H:3]1[CH2:8][NH:7][CH2:6][CH2:5][N:4]1[C:16]([O:18][C:19]([CH3:20])([CH3:22])[CH3:21])=[O:17])[CH3:2]
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참가 물질

4

반응물 1

HCID 20598790(2S)-2-Ethyl-4-(phenylmethyl)-1-piperazinecarboxylic acid, 1,1-dimethylethyl ester

생성물 1

HCID 17750462(S)-2-Ethylpiperazine, N1-BOC protected

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A solution of the product from example 69 part c) (6.09 g) and 10% Pd/C (1.14 g) in EtOH (85 mL) was hydrogenated at 3.8 bar for 16 h. The reaction mixture was filtered through Celite and the filtrate concentrated in vacuo to give the sub-title compound as an oil (3.65 g).

후처리

  1. filtrationThe reaction mixture was filtered through Celite
  2. concentrationthe filtrate concentrated in vacuo

출처 및 근거

ORD 기록
ord-5216b17b5e254935a2298eed40070471
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08524715B2

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