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2-{[(3-Methoxypyridin-2-yl)methyl]sulfanyl}ethan-1-amine → HCID 70509255, 화합물

HRID 263238
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반응식

HRID 263238 반응식
[NH2:1][CH2:2][CH2:3][S:4][CH2:5][C:6]1[C:11]([O:12][CH3:13])=[CH:10][CH:9]=[CH:8][N:7]=1.[CH3:14][S:15][C:16](S(C)=O)=[CH:17][N+:18]([O-:20])=[O:19]>CO>[CH3:14][S:15][C:16]([NH:1][CH2:2][CH2:3][S:4][CH2:5][C:6]1[C:11]([O:12][CH3:13])=[CH:10][CH:9]=[CH:8][N:7]=1)=[CH:17][N+:18]([O-:20])=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 129515352-{[(3-Methoxypyridin-2-yl)methyl]sulfanyl}ethan-1-amineHCID 544870941-Nitro2-methylthio-2-methylsulphinylethylene

생성물 1

HCID 70509255HCID 70509255, 화합물수율 56.9%

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

A solution of 2-[2-aminoethylthiomethyl]-3-methoxypyridine (2.1 g) in methanol (33 ml) was added over 25 minutes to a stirred solution of 1-methylthio-1-methylsulphinyl-2nitroethylene (2.1 g) in methanol (75 ml) at 30°. After standing for an hour the solution was concentrated to give a yellow-brown oil which was crystallised from ethanol/ether to yield 1-methylthio-1-[2-((3-methoxy-2-pyridyl)methylthio)ethylamino]-2-nitroethylene (1.9 g), m.p. 87.5°-88.5°.

후처리

  1. waitAfter standing for an hour
  2. concentrationthe solution was concentrated
  3. customto give a yellow-brown oil which
  4. customwas crystallised from ethanol/ether

출처 및 근거

ORD 기록
ord-5dfbe08c0ca54d1baf7f6999195c40f3
출처 데이터셋
uspto-grants-1979_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04156727

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