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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethylamine → 6-(Ethylamino)pyridazine-3-carboxamide

HRID 840305
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HRID 840305 반응식
Cl[C:2]1[N:7]=[N:6][C:5]([C:8]([NH2:10])=[O:9])=[CH:4][CH:3]=1.[CH2:11]([NH2:13])[CH3:12]>CO>[CH2:11]([NH:13][C:2]1[N:7]=[N:6][C:5]([C:8]([NH2:10])=[O:9])=[CH:4][CH:3]=1)[CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6341EthylamineHCID 125775576-Chloropyridazine-3-carboxamide

생성물 1

HCID 226225026-(Ethylamino)pyridazine-3-carboxamide

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A suspension of 6-chloropyridazine-3-carboxamide (28.5 g, 0.18 mol) in methanol (200 ml) was treated with aqueous ethylamine (70% solution, 77 ml). The reaction was heated at reflux for 3½ hours. The reaction was allowed to cool to ambient temperature and stand overnight. The precipitate was filtered and washed with a small volume of water and dried to give 6-(ethylamino)pyridazine-3-carboxamide as pink solid (8.9 g). [The filtrates were evaporated to a small volume diluted with cold water (100 ml) and more of the desired solid was filtered-off, washed with water and dried (12.8 g). Total yield (21.7 g, 72%)].

후처리

  1. temperatureThe reaction was heated
  2. temperatureat reflux for 3½ hours
  3. filtrationThe precipitate was filtered
  4. washwashed with a small volume of water
  5. customdried

출처 및 근거

ORD 기록
ord-ffd723eb35d54d59a36e3287e93a870a
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06365603B1

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