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Methyl triflate → N-[2-(pyridin-2-ylsulfanyl)ethyl)thioacetimidic acid methyl ester

HRID 2224748
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HRID 2224748 반응식
F[C:2](F)(F)S(OC)(=O)=O.[N:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[S:16][CH2:17][CH2:18][NH:19][C:20](=[S:22])[CH3:21]>C(Cl)Cl>[CH3:2][S:22][C:20](=[N:19][CH2:18][CH2:17][S:16][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][N:10]=1)[CH3:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 9526Methyl triflateHCID 86607043N-(2-(pyridin-2-ylsulfanyl)ethyl)thioacetamide

생성물 1

HCID 69317476N-[2-(pyridin-2-ylsulfanyl)ethyl)thioacetimidic acid methyl ester수율 100%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Add methyl trifluoromethanesulfonate (65.5 mg, 0.4 mmol) to a solution of N-(2-(pyridin-2-ylsulfanyl)ethyl)thioacetamide (85.0 mg, 0.4 mmol) in methylene chloride (10 mL) under nitrogen. Stir the reaction mixture at room temperature for 5 minutes and remove the solvent under reduced pressure to give N-[2-(pyridin-2-ylsulfanyl)ethyl)thioacetimidic acid methyl ester (0.4 mmol) as a colorless oil. MS (ES): m/z 227 (M+H).

후처리

  1. customremove the solvent under reduced pressure

출처 및 근거

ORD 기록
ord-89fda9096085474099d5ac82eef158e6
출처 데이터셋
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07378447B2

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