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Methanol → N-(2-chloro-4-sulfamoylphenyl)-4-methoxypiperidine-1-carboxamide

HRID 2040344
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반응식

HRID 2040344 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([S:11]([NH2:14])(=[O:13])=[O:12])[CH:5]=[CH:6][C:7]=1[N:8]=[C:9]=[O:10].[CH3:15][O:16][CH:17]1[CH2:22][CH2:21][NH:20][CH2:19][CH2:18]1.CO>O1CCCC1>[Cl:1][C:2]1[CH:3]=[C:4]([S:11](=[O:12])(=[O:13])[NH2:14])[CH:5]=[CH:6][C:7]=1[NH:8][C:9]([N:20]1[CH2:21][CH2:22][CH:17]([O:16][CH3:15])[CH2:18][CH2:19]1)=[O:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 776664-MethoxypiperidineHCID 866536933-Chloro-4-isocyanatobenzenesulfonamide

생성물 1

HCID 67126739N-(2-chloro-4-sulfamoylphenyl)-4-methoxypiperidine-1-carboxamide

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
60 °C

실험 절차

To a solution of EXAMPLE 392A in anhydrous tetrahydrofuran (6 mL) was added 4-methoxypiperidine (451 mg). The mixture was stirred at 60° C. for 3 hours. The mixture was cooled, mixed with methanol (20 mL) and silica gel (6 g) and concentrated. The material was purified on a silica gel column and was eluted with 10% methanol in dichloromethane to provide the title compound.

후처리

  1. temperatureThe mixture was cooled
  2. concentrationconcentrated
  3. customThe material was purified on a silica gel column
  4. washwas eluted with 10% methanol in dichloromethane

출처 및 근거

ORD 기록
ord-8cdf913c37914fdb94b260c67ac55347
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08580794B2

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