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Hydrochloric Acid → SULFONILAMIDE,N-(4-INDOLYL)

HRID 1585727
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HRID 1585727 반응식
[NH:1]1[C:9]2[C:4](=[C:5]([NH:10][S:11]([C:14]3[CH:19]=[CH:18][C:17]([NH:20]C(=O)C)=[CH:16][CH:15]=3)(=[O:13])=[O:12])[CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.Cl>[OH-].[Na+]>[NH2:20][C:17]1[CH:18]=[CH:19][C:14]([S:11]([NH:10][C:5]2[CH:6]=[CH:7][CH:8]=[C:9]3[C:4]=2[CH:3]=[CH:2][NH:1]3)(=[O:13])=[O:12])=[CH:15][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 19601792HCID 19601792, 화합물

생성물 1

HCID 10637020SULFONILAMIDE,N-(4-INDOLYL)수율 66%

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

실험 절차

0.15 g (0.00045 mol) of N-[4-(1H-indol-4-ylsulfamoyl)-phenyl]-acetamide was dissolved in 4 ml of 1N NaOH and boiled at reflux for 1 hour. After cooling the mixture was adjusted to pH 6 with 0.1N HCl and the precipitate which separated was filtered off. The material on the suction filter was washed with copious water and dried. It was subsequently chromatographed on silica gel with ethyl acetate/hexane 1:1. There was obtained 0.085 g (66%) of 4-amino-N-(1H-indol-4-yl)-benzenesulfonamide as a white amorphous solid; m.p.: 215° C.

후처리

  1. temperatureat reflux for 1 hour
  2. temperatureAfter cooling the mixture
  3. customthe precipitate which separated
  4. filtrationwas filtered off
  5. filtrationThe material on the suction filter
  6. washwas washed with copious water
  7. customdried
  8. customIt was subsequently chromatographed on silica gel with ethyl acetate/hexane 1:1

출처 및 근거

ORD 기록
ord-502d2b029ad4439982fcb9f90ae19e4a
출처 데이터셋
uspto-grants-1999_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05939451

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