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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethanol → Methyl 4-morpholinethiocarboximidate hydroiodide

HRID 128068
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HRID 128068 반응식
[N:1]1([C:7](=[S:9])[NH2:8])[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[I:10]C.[CH2:12](O)C>CCOCC>[IH:10].[N:1]1([C:7]([S:9][CH3:12])=[NH:8])[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702EthanolHCID 6328Methyl iodideHCID 23935444-Morpholinecarbothioamide

생성물 1

HCID 16333240Methyl 4-morpholinethiocarboximidate hydroiodide

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

A solution of 4.65 g. of 4-morpholinethiocarboxamide [W. G. Finnegan, et al., J. Org. Chem. 18, 779 (1952)] and 4.54 g. of iodomethane in 50 ml. of ethanol is allowed to stand 48 hours at room temperature, then diluted with 250 ml. of ether to give a colorless crystalline precipitate of methyl 4-morpholinethiocarboximidate hydroiodide. A solution of 5.76 g. of this product and 1.1 g. of hydrazine hydrate in ethanol is heated under reflux for about 2 hours and then treated with 2.1 g. of 9,10-anthracenedicarboxaldehyde in 200 ml. of ethanol and 2 ml. of glacial acetic acid by heating under reflux for 3.5 hours. The solution is filtered and then evaporated to give an orange solid which is recrystallized from ethanol-ether to give the title compound, m.p. 280° C.

후처리

  1. additiondiluted with 250 ml

출처 및 근거

ORD 기록
ord-31a320262aa54209a4f7df096b27985a
출처 데이터셋
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04258181

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