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

Acetone → HCID 13343851, 화합물

HRID 365301
노트
인쇄 미리보기

반응식

HRID 365301 반응식
[OH:1][C:2]1[CH:12]=[CH:11][C:5]2[NH:6][C:7](=[O:10])[CH2:8][S:9][C:4]=2[CH:3]=1.Br[CH2:14][CH2:15][CH2:16][Cl:17].CC(C)=O>>[Cl:17][CH2:16][CH2:15][CH2:14][O:1][C:2]1[CH:12]=[CH:11][C:5]2[NH:6][C:7](=[O:10])[CH2:8][S:9][C:4]=2[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 180AcetoneHCID 80061-Bromo-3-chloropropaneHCID 8200317-hydroxy-2H-1,4-benzothiazin-3(4H)-one

생성물 1

HCID 13343851HCID 13343851, 화합물수율 50.4%

실험 절차

After a mixture consisting of 7-hydroxy-3,4-dihydro-2H-1,4-benzothiazin-3-one (1.812 g, 10 mmol), 1bromo-3-chloropropane (2.362 g, 15 mmol), potassium carbate (4.146 g, 30 mmol) and acetone (40 mmol) was heated under reflux and stirring for 24 hours, insolube matter was filtered off, and the solvent was distilled off under reduced pressure. The residue was subjected to chromatography on a silica gel column (developer: chloroform) to purify the same, and was then recrystallized from acetone. The title compound (1.300 g) was obtained as yellow leaflets (yield: 50.4%).

후처리

  1. temperaturewas heated
  2. temperatureunder reflux
  3. filtrationinsolube matter was filtered off
  4. distillationthe solvent was distilled off under reduced pressure
  5. customto purify the same, and
  6. customwas then recrystallized from acetone

출처 및 근거

ORD 기록
ord-cbbf3a06c7d04efaab9b011975b2bcaf
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06127360

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트