홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Hydrochloric Acid → 5-amino-1-(2-hydroxyethyl)-1H-pyrazole-4-carbaldehyde

HRID 349547
노트
인쇄 미리보기

반응식

HRID 349547 반응식
[NH2:1][C:2]1[N:6]([CH2:7][CH2:8][OH:9])[N:5]=[CH:4][C:3]=1[C:10]#N.Cl.C[OH:14]>[C].[Pd]>[NH2:1][C:2]1[N:6]([CH2:7][CH2:8][OH:9])[N:5]=[CH:4][C:3]=1[CH:10]=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 887MethanolHCID 2198525-amino-1-(2-hydroxyethyl)-1H-pyrazole-4-carbonitrile

생성물 1

HCID 179620345-amino-1-(2-hydroxyethyl)-1H-pyrazole-4-carbaldehyde

시약·촉매·용매 1

HCID 178418390HCID 178418390, 화합물촉매

실험 절차

To a solution of 5-amino-1-(2-hydroxyethyl)-1H-pyrazole-4-carbonitrile (15 g) in methanol (300 ml) was added hydrochloric acid (1.8 ml) under ice-cooling. The resulting solution was stirred for 15 minutes. The mixture was treated with 10% palladium carbon (7.5 g) under a hydrogen atmosphere at room temperature for 3 hours. After the catalyst was filtered off, the filtrate was concentrated in vacuo to give 5-amino-1-(2-hydroxyethyl)-1H-pyrazole-4-carbaldehyde (13.3 g).

후처리

  1. temperaturecooling
  2. filtrationAfter the catalyst was filtered off
  3. concentrationthe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-67e106826f9c4d3fac004ef6ef0484cf
출처 데이터셋
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07179801B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트