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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Cysteamine → 6-Methyl-3-pyridylmethyl-4-pyrimidone

HRID 67878
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인쇄 미리보기

반응식

HRID 67878 반응식
C[N:2]([CH2:4][C:5]1O[C:8]([CH2:10]O)=[CH:7][CH:6]=1)[CH3:3].CN(CC1[O:20]C(CSCCN)=CC=1)C.NCCS.[NH2:30][CH2:31][CH2:32][C:33]1[N:37]=CN[CH:34]=1.[H][H]>C(O)(=O)C>[CH3:34][C:33]1[N:37]=[C:10]([CH2:8][C:7]2[CH:3]=[N:2][CH:4]=[CH:5][CH:6]=2)[NH:30][C:31](=[O:20])[CH:32]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6058CysteamineHCID 849065-((Dimethylamino)methyl)-2-furanmethanolHCID 1622035-(((2-Aminoethyl)thio)methyl)-N,N-dimethyl-2-furanmethanamineHCID 178510869HCID 178510869, 화합물

생성물 1

HCID 1361872966-Methyl-3-pyridylmethyl-4-pyrimidone

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

5-Dimethylaminomethyl-2-furanmethanol can be converted into 2-(5-dimethylaminomethyl-2-furanylmethylthio)ethylamine by heating under reflux in acetic acid with cysteamine and can be further converted into various histamine H2 -antagonists for example, by reacting with a substituted pyrimidone to give 2-2-(5-dimethylaminomethyl-2-furanylmethylthio)ethylamino-5-(6-methyl-3-pyridylmethyl-4-pyrimidone by methods described in EP 3677.

후처리

  1. temperatureby heating

출처 및 근거

ORD 기록
ord-3bde087f247843d19e16bfe9b8309d82
출처 데이터셋
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04347191

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