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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 14476487, 화합물 → HCID 14476489, 화합물

HRID 1904950
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HRID 1904950 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[N:8](S(C1C=CC=CC=1)(=O)=O)[C:7]([S:21](=[O:24])(=[O:23])[NH2:22])=[CH:6]2>[OH-].[Na+]>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7]([S:21](=[O:24])(=[O:23])[NH2:22])=[CH:6]2
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 14476487HCID 14476487, 화합물

생성물 1

HCID 14476489HCID 14476489, 화합물수율 4,647.7%

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

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온도
90 °C

실험 절차

5-methoxy-1-benzenesulfonyl-2-sulfamoylindole (22.0 gm, 0.97 mmol) was dissolved in 10% sodium hydroxide (250 ml) and warmed to 90° C. for 1 hour. The cooled reaction mixture was extracted with ethyl acetate (2×150 ml) and neutralized with concentrated hydrochloric acid. The precipitate was collected via filtration and the filtrate was extracted with ethyl acetate (4×200 ml). The precipitate collected earlier was combined with the extracts and the extracts were washed with water (2×100 ml), brine (2×100 ml) and dried (MgSO4). The organic solvent was removed under vacuum to yield a brown solid 10.2 gm. The solid was recrystallized from water using decolorizing carbon to yield white crystals; 4.5 gm., m.p. 208°-209° C.

후처리

  1. customThe cooled reaction mixture
  2. extractionwas extracted with ethyl acetate (2×150 ml) and neutralized with concentrated hydrochloric acid
  3. filtrationThe precipitate was collected via filtration
  4. extractionthe filtrate was extracted with ethyl acetate (4×200 ml)
  5. customThe precipitate collected earlier
  6. washthe extracts were washed with water (2×100 ml), brine (2×100 ml)
  7. dry with materialdried (MgSO4)
  8. customThe organic solvent was removed under vacuum

출처 및 근거

ORD 기록
ord-075b65bcb9464b2d9b137a1133d34874
출처 데이터셋
uspto-grants-1989_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04840963

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