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Dimethyl N-cyanodithioiminocarbonate → HCID 20316728, 화합물

HRID 1974420
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인쇄 미리보기

반응식

HRID 1974420 반응식
[NH2:1][CH2:2][CH2:3][S:4][CH2:5][C:6]1[C:11]([OH:12])=[CH:10][CH:9]=[CH:8][N:7]=1.[CH3:13][S:14][C:15](=[N:18][C:19]#[N:20])SC>C(O)C>[C:19]([NH:18][C:15](=[N:1][CH2:2][CH2:3][S:4][CH2:5][C:6]1[C:11]([OH:12])=[CH:10][CH:9]=[CH:8][N:7]=1)[S:14][CH3:13])#[N:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 66289Dimethyl N-cyanodithioiminocarbonateHCID 129515342-{[(2-Aminoethyl)sulfanyl]methyl}pyridin-3-OL

생성물 1

HCID 20316728HCID 20316728, 화합물수율 42.2%

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

A solution of 2-((2-aminoethyl)thiomethyl)-3-hydroxypyridine (7.5 g) in ethanol was added slowly to a solution of dimethylcyanodithioimidocarbonate (6.0 g) in ethanol, with stirring at room temperature. The mixture was set aside overnight at room temperature. Filtration afforded N-cyano-N'-[2-((3-hydroxy-2-pyridyl)methylthio)-ethyl]-S-methylisothiourea (4.85 g), m.p. 192°-194°. Recrystallisation from aqueous ethanol gave fine needles, m.p. 196°-198°.

후처리

  1. filtrationFiltration

출처 및 근거

ORD 기록
ord-fd0d436fc5fb43ec89fe444dc5945bc4
출처 데이터셋
uspto-grants-1976_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04000302

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