Dichloromethane → N-[Chloro-4-(tetrahydro-pyran-2-yloxy)-benzyl]-3-methyl-N-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-benzamide

HRID 1827539노트

반응식

HRID 1827539 반응식
Cl[C:2]1[CH:23]=[C:22]([O:24][CH:25]2[CH2:30][CH2:29][CH2:28][CH2:27][O:26]2)[CH:21]=[CH:20][C:3]=1[CH2:4][NH:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][CH2:13][CH2:14][N:15]2[CH2:19][CH2:18][CH2:17][CH2:16]2)=[CH:8][CH:7]=1.C(N(CC)CC)C.[C:38]1([CH3:47])[CH:43]=[CH:42][CH:41]=[C:40]([C:44](Cl)=[O:45])[CH:39]=1.C(=O)(O)[O-].[Na+].C(Cl)[Cl:54]>>[Cl:54][CH:4]([N:5]([C:6]1[CH:11]=[CH:10][C:9]([O:12][CH2:13][CH2:14][N:15]2[CH2:19][CH2:18][CH2:17][CH2:16]2)=[CH:8][CH:7]=1)[C:44](=[O:45])[C:40]1[CH:41]=[CH:42][CH:43]=[C:38]([CH3:47])[CH:39]=1)[C:3]1[CH:20]=[CH:21][C:22]([O:24][CH:25]2[CH2:30][CH2:29][CH2:28][CH2:27][O:26]2)=[CH:23][CH:2]=1

참가 물질

6

실험 절차

A solution of [2-chloro-4-(tetrahydro-pyran-2-yloxy)-benzyl]-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-amine (100 mg, 0.232 mmol) and triethylamine (0.100 mL, 0.696 mmol) in methylene chloride was added to m-toluenecarbonyl chloride (72 mg, 0.46 mmol). The reaction mixture was stirred at room temperature for 24 hr. Saturated aqueous sodium bicarbonate was added and the layers were separated. The aqueous layer was washed with 2 mL of methylene chloride. The combined organic layers were concentrated to give the title compound of Step A. MS 549.1 (M+1)+

후처리

  1. customthe layers were separated
  2. washThe aqueous layer was washed with 2 mL of methylene chloride
  3. concentrationThe combined organic layers were concentrated

출처 및 근거

ORD 기록
ord-5c80da1d9bd64702a1a6287a0ee3f4a1
출처 데이터셋
uspto-grants-2006_05
특허 번호
US07053212B2

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