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Thionyl Chloride → 4-[chloro(8-quinolinyl)methyl]-N,N-diethylbenzamide

HRID 1837544
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인쇄 미리보기

반응식

HRID 1837544 반응식
[CH2:1]([N:3]([CH2:24][CH3:25])[C:4](=[O:23])[C:5]1[CH:10]=[CH:9][C:8]([CH:11](O)[C:12]2[CH:13]=[CH:14][CH:15]=[C:16]3[C:21]=2[N:20]=[CH:19][CH:18]=[CH:17]3)=[CH:7][CH:6]=1)[CH3:2].O=S(Cl)[Cl:28]>C(Cl)Cl>[Cl:28][CH:11]([C:12]1[CH:13]=[CH:14][CH:15]=[C:16]2[C:21]=1[N:20]=[CH:19][CH:18]=[CH:17]2)[C:8]1[CH:9]=[CH:10][C:5]([C:4]([N:3]([CH2:24][CH3:25])[CH2:1][CH3:2])=[O:23])=[CH:6][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 10711782N,N-diethyl-4-[hydroxy(8-quinolinyl)methyl]benzamide

생성물 1

HCID 226778764-[chloro(8-quinolinyl)methyl]-N,N-diethylbenzamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
25 °C

실험 절차

Compound II (2.0 g, 6.6 mmol) was dissolved in dry CH2Cl2 (25 mL) and SOCl2 (0.53 mL, 7.3 mmol) was added. The solution was stirred at 25° C. for 30 min and the solvent was evaporated in vacuo. Compound III was obtained as an oil (˜100%) and used in the next reaction without further purification.

후처리

  1. customthe solvent was evaporated in vacuo

출처 및 근거

ORD 기록
ord-5f23844e816b40e9b87f1363ec549fcb
출처 데이터셋
uspto-grants-2004_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06784181B2

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