N-(3-Aminopropyl)morpholine → 3-({1-[bis(4-chlorophenyl)methyl]azetidin-3-ylidene} methanesulfonylmethyl)-N-(3-morpholin-4-ylpropyl)benzamide

HRID 25207

반응식

HRID 25207 반응식
[NH2:1][CH2:2][CH2:3][CH2:4][N:5]1[CH2:10][CH2:9][O:8][CH2:7][CH2:6]1.[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([CH:18]([C:37]2[CH:42]=[CH:41][C:40]([Cl:43])=[CH:39][CH:38]=2)[N:19]2[CH2:22][C:21](=[CH:23][S:24]([CH2:27][C:28]3[CH:29]=[C:30]([CH:34]=[CH:35][CH:36]=3)[C:31](O)=[O:32])(=[O:26])=[O:25])[CH2:20]2)=[CH:14][CH:13]=1>ClCCl>[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([CH:18]([C:37]2[CH:38]=[CH:39][C:40]([Cl:43])=[CH:41][CH:42]=2)[N:19]2[CH2:22][C:21](=[CH:23][S:24]([CH2:27][C:28]3[CH:29]=[C:30]([CH:34]=[CH:35][CH:36]=3)[C:31]([NH:1][CH2:2][CH2:3][CH2:4][N:5]3[CH2:10][CH2:9][O:8][CH2:7][CH2:6]3)=[O:32])(=[O:26])=[O:25])[CH2:20]2)=[CH:14][CH:13]=1

참가 물질

4

실험 절차

0.0388 cm3 of N-(3-aminopropyl)morpholine is added, at the same temperature, to a suspension of 150 mg of 3-({1-[bis(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)benzoic acid activated on TFP resin (165 μM) in 3 cm3 of dichloromethane, pre-stirred for 90 minutes at a temperature close to 20° C. The suspension is stirred at a temperature close to 20° C. for 22 hours and then filtered on sintered glass. The solid residue is rewashed with twice 1.5 cm3 of dichloromethane. The filtrates are combined and concentrated to dryness under reduced pressure (2.7 kPa) at a temperature close to 40° C. 60 mg of 3-({1-[bis(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)-N-(3-morpholin-4-ylpropyl)benzamide are thus obtained in the form of a pale yellow foam.

후처리

  1. customclose to 20° C
  2. stirringThe suspension is stirred at a temperature
  3. customclose to 20° C. for 22 hours
  4. filtrationfiltered on sintered glass
  5. concentrationconcentrated to dryness under reduced pressure (2.7 kPa) at a temperature
  6. customclose to 40° C

출처 및 근거

ORD 기록
ord-4634c880f5ca4716bd33fcdc4904024b
출처 데이터셋
uspto-grants-2005_02
특허 번호
US06858603B2

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