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

Nicotinic acid, hydrazide → N-[[(E)-but-2-enylidene]amino]pyridine-3-carboxamide

HRID 330353
노트
인쇄 미리보기

반응식

HRID 330353 반응식
[C:1]([NH:9][NH2:10])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[N:4][CH:3]=1.[CH:11](=O)/[CH:12]=[CH:13]/[CH3:14]>CO>[C:1]([NH:9][N:10]=[CH:11]/[CH:12]=[CH:13]/[CH3:14])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[N:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 11112Nicotinic acid, hydrazideHCID 447466Crotonaldehyde

생성물 1

HCID 67834889N-[[(E)-but-2-enylidene]amino]pyridine-3-carboxamide

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

In 50 ml of methanol was suspended 22 g of nicotinic acid hydrazide. To the suspension was added dropwise 13.2 ml of crotonaldehyde, followed by stirring for 30 minutes at room temperature. Methanol was distilled away under reduced pressure, and the residue washed with ether, filtered off, and dried. Thus there was obtained 27.5 g of crotonaldehyde nicotinoyl hydrazone (mp. 144°-145° C.).

후처리

  1. distillationMethanol was distilled away under reduced pressure
  2. washthe residue washed with ether
  3. filtrationfiltered off
  4. customdried

출처 및 근거

ORD 기록
ord-1faba2d266cf4df2a6d6cb869e38a700
출처 데이터셋
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04895947

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트