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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Propylamine → 5-Chloro-6-n-propylsulfamoyl-1-indanone

HRID 65934
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인쇄 미리보기

반응식

HRID 65934 반응식
[CH2:1]([NH2:4])[CH2:2][CH3:3].C(N(CC)CC)C.[Cl:12][C:13]1[CH:14]=[C:15]2[C:19](=[CH:20][C:21]=1[S:22](Cl)(=[O:24])=[O:23])[C:18](=[O:26])[CH2:17][CH2:16]2>CC(C)=O>[Cl:12][C:13]1[CH:14]=[C:15]2[C:19](=[CH:20][C:21]=1[S:22](=[O:23])(=[O:24])[NH:4][CH2:1][CH2:2][CH3:3])[C:18](=[O:26])[CH2:17][CH2:16]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7852PropylamineHCID 8471TriethylamineHCID 221190346-chloro-3-oxo-2,3-dihydro-1H-indene-5-sulfonyl chloride

생성물 1

HCID 227563895-Chloro-6-n-propylsulfamoyl-1-indanone

시약·촉매·용매 1

HCID 180Acetone용매2회

실험 절차

A solution of 1.95 g (33 mmoles) of n-propylamine and 3.04 g (30 mmoles) of triethylamine in 50 ml of acetone is added to a solution of 7.95 g (30 mmoles) of 5-chloro-6-chlorosulfonyl-1-indanone in 50 ml of acetone, and the whole is stirred for 6 hours at room temperature, thereafter for 1 hour at boiling temperature. The solution is largely concentrated, 200 ml of water are added, and the mixture is then acidified with 2N hydrochloric acid to a pH of 2. The precipitate is filtered off with suction and washed with water. The product melts at 122° to 123° C.

후처리

  1. waitfor 1 hour at boiling
  2. concentrationThe solution is largely concentrated
  3. addition200 ml of water are added
  4. filtrationThe precipitate is filtered off with suction
  5. washwashed with water

출처 및 근거

ORD 기록
ord-1b2fe95f2bff4408ab484d41b09ebfc3
출처 데이터셋
uspto-grants-1978_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04129656

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