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Methyl triflate → 1-Methyl-3-(piperidine-1-sulfonyl)-3h-imidazol-1-ium triflate salt

HRID 2089711
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인쇄 미리보기

반응식

HRID 2089711 반응식
[N:1]1([S:6]([N:9]2[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]2)(=[O:8])=[O:7])[CH:5]=[CH:4][N:3]=[CH:2]1.[O:15](C)[S:16]([C:19]([F:22])([F:21])[F:20])(=[O:18])=[O:17]>C(Cl)Cl>[O-:18][S:16]([C:19]([F:22])([F:21])[F:20])(=[O:17])=[O:15].[CH3:19][N+:3]1[CH:4]=[CH:5][N:1]([S:6]([N:9]2[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]2)(=[O:8])=[O:7])[CH:2]=1
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참가 물질

4

반응물 2

HCID 9526Methyl triflateHCID 29901621-(Imidazole-1-sulfonyl)-piperidine

생성물 1

HCID 873994191-Methyl-3-(piperidine-1-sulfonyl)-3h-imidazol-1-ium triflate salt

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of compound 1-H (79.6 mg, 0.37 mmol) in CH2Cl2 (2 mL), cooled to 0° C., was added methyl triflate (46 μL, 0.407 mmol). The reaction mixture was allowed to warm to ambient temperature and stirred for 3 hours. The solvent was evaporated under reduced pressure to afford compound 1-I as a white solid. MS (method 2): m/z 229.9 (MH+).

후처리

  1. customThe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-ed3a3cc8c78b440eb57a6688b2ecfa48
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08436041B2

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