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Triethylamine → 3-Methoxy-N-(1-methylazetidin-3-yl)-4-nitrobenzamide

HRID 1487648
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반응식

HRID 1487648 반응식
[CH3:1][N:2]1[CH2:5][CH:4]([NH2:6])[CH2:3]1.C(N(CC)CC)C.[CH3:14][O:15][C:16]1[CH:17]=[C:18]([CH:22]=[CH:23][C:24]=1[N+:25]([O-:27])=[O:26])[C:19](Cl)=[O:20]>C(Cl)Cl>[CH3:14][O:15][C:16]1[CH:17]=[C:18]([CH:22]=[CH:23][C:24]=1[N+:25]([O-:27])=[O:26])[C:19]([NH:6][CH:4]1[CH2:5][N:2]([CH3:1])[CH2:3]1)=[O:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 111276553-methoxy-4-nitro-benzoyl ChlorideHCID 187126621-Methylazetidin-3-amine

생성물 1

HCID 867264813-Methoxy-N-(1-methylazetidin-3-yl)-4-nitrobenzamide수율 46.4%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a solution of 1-methylazetidin-3-amine (1 equiv) in dry DCM (0.13 M) was added triethylamine (1.8 equiv). A solution of 3-methoxy-4-nitrobenzoyl chloride (0.91 equiv) in dry DCM was added and the reaction was stirred at room temperature for 5 min. The mixture was then concentrated and purified by silica gel chromatography (5% MeOH in DCM) to afford the title compound (46.4% yield) as a yellow solid. MS (ESI) m/z 266.1 [M+H]+.

후처리

  1. concentrationThe mixture was then concentrated
  2. custompurified by silica gel chromatography (5% MeOH in DCM)

출처 및 근거

ORD 기록
ord-4052af470ca04efbbef86e4bea4225e2
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09428509B2

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