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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 20191014, 화합물 → HCID 20191013, 화합물

HRID 2119127
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HRID 2119127 반응식
[OH:1][CH:2]([CH2:9][CH2:10][N:11]1[CH:15]=[CH:14][C:13]([N+:16]([O-])=O)=[N:12]1)[CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5]>CO.[Pd].[C]>[OH:1][CH:2]([CH2:9][CH2:10][N:11]1[CH:15]=[CH:14][C:13]([NH2:16])=[N:12]1)[CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 20191014HCID 20191014, 화합물

생성물 1

HCID 20191013HCID 20191013, 화합물

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 887Methanol용매

실험 절차

A solution of the above crude ethyl 3-hydroxy-5-(3-nitropyrazol-1-yl)valerate (2.41 g.) in MeOH (250 ml.) was hydrogenated over 5% w/w Pd/carbon (0.3 g.) at atmospheric pressure over 2 hours. Uptake was 650 ml. The catalyst was filtered off and the filtrate was evaporated in vacuo to give ethyl 3-hydroxy-5-(3-aminopyrazol-1-yl)valerate as an oil (1.47 g.).

후처리

  1. filtrationThe catalyst was filtered off
  2. customthe filtrate was evaporated in vacuo

출처 및 근거

ORD 기록
ord-00114f9bf32b4659a7059ae08b98bb83
출처 데이터셋
uspto-grants-1987_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04683228

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