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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 13472255, 화합물 → HCID 13472256, 화합물

HRID 1247862
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HRID 1247862 반응식
CC([NH:5][S:6]([C:9]1[C:17]2[CH2:16][S:15][CH2:14][C:13]=2[CH:12]=[CH:11][CH:10]=1)(=[O:8])=[O:7])(C)C>FC(F)(F)C(O)=O.CCCCCC.C(OCC)(=O)C>[CH2:14]1[C:13]2[CH:12]=[CH:11][CH:10]=[C:9]([S:6]([NH2:5])(=[O:7])=[O:8])[C:17]=2[CH2:16][S:15]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 13472255HCID 13472255, 화합물

생성물 1

HCID 13472256HCID 13472256, 화합물수율 58.8%

시약·촉매·용매 2

HCID 6422Trifluoroacetic acid용매HCID 21226206Ethyl acetate hexane용매

실험 절차

A solution of 3.0 g of 1,3-dihydro-N-(1,1-dimethylethyl)benzo[c]thiophene-4-sulfonamide in 50 ml of trifluoroacetic acid was stirred at ambient temperature for 4 hours. The brown solution was concentrated in vacuo. 1-Chlorobutane was added to the resulting brown oil and the mixture concentrated in vacuo. Repeating this procedure gave an oil which on trituration with 1-chlorobutane gave a brown solid. Purification of the crude reaction product by chromatography, using hexane/ethyl acetate (3:2) as eluent gave 1.4 g of 1,3-dihydrobenzo[c]thiophene-4-sulfonamide as a pale yellow solid, m.p. 146°-148°.

후처리

  1. concentrationThe brown solution was concentrated in vacuo
  2. addition1-Chlorobutane was added to the resulting brown oil
  3. concentrationthe mixture concentrated in vacuo
  4. customRepeating this procedure gave an oil which on trituration with 1-chlorobutane
  5. customgave a brown solid
  6. customPurification of the crude
  7. customreaction product by chromatography

출처 및 근거

ORD 기록
ord-77aabde2d5f54969a2355cab9e13982a
출처 데이터셋
uspto-grants-1985_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04521241

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