홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Hydrochloric Acid → N-(2,4-dimethoxybenzyl)-3,4-difluorobenzenesulfonamide

HRID 337732
노트
인쇄 미리보기

반응식

HRID 337732 반응식
[CH3:1][O:2][C:3]1[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[CH:7][C:4]=1[CH2:5][NH2:6].N1C=CC=CC=1.[F:19][C:20]1[CH:21]=[C:22]([S:27](Cl)(=[O:29])=[O:28])[CH:23]=[CH:24][C:25]=1[F:26].Cl>ClCCl>[CH3:1][O:2][C:3]1[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[CH:7][C:4]=1[CH2:5][NH:6][S:27]([C:22]1[CH:23]=[CH:24][C:25]([F:26])=[C:20]([F:19])[CH:21]=1)(=[O:29])=[O:28]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 1049PyridineHCID 5972502,4-DimethoxybenzylamineHCID 27369133,4-Difluorobenzene-1-sulfonyl chloride

생성물 1

HCID 89962551N-(2,4-dimethoxybenzyl)-3,4-difluorobenzenesulfonamide수율 100%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

실험 절차

To a solution of 2,4-dimethoxybenzylamine (3.35 mL, 22.3 mmol) and pyridine (9.02 mL, 111.5 mmol) in dichloromethane (75 mL), 3,4-difluorobenzenesulfonyl chloride (3.04 mL, 22.3 mmol) was added with cooling on ice, and the reaction solution was stirred at room temperature for 16 hours. To the reaction solution, 2 M hydrochloric acid (100 mL) was added, and an organic layer was extracted. The thus obtained organic layer was dried over anhydrous sodium sulfate and vacuum concentrated to yield the title compound (7.66 g, 99%) as a colorless solid.

후처리

  1. temperaturewith cooling on ice
  2. extractionan organic layer was extracted
  3. dry with materialThe thus obtained organic layer was dried over anhydrous sodium sulfate and vacuum
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-96b055b881cc4de09baae01a2ea3a2b1
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08889741B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트