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HCID 21528841, 화합물 → Benzenesulfonamide, 3-chloro-4-(2,5-dioxo-3-phenyl-1-imidazolidinyl)-

HRID 1658213
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HRID 1658213 반응식
[C:1]([N:4]([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[CH2:5][C:6]([NH:8][C:9]1[CH:14]=[CH:13][C:12]([S:15](=[O:18])(=[O:17])[NH2:16])=[CH:11][C:10]=1[Cl:19])=[O:7])(O)=[O:2]>C(OC(=O)C)(=O)C>[C:20]1([N:4]2[CH2:5][C:6](=[O:7])[N:8]([C:9]3[CH:14]=[CH:13][C:12]([S:15](=[O:18])(=[O:17])[NH2:16])=[CH:11][C:10]=3[Cl:19])[C:1]2=[O:2])[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 21528841HCID 21528841, 화합물

생성물 1

HCID 3041008Benzenesulfonamide, 3-chloro-4-(2,5-dioxo-3-phenyl-1-imidazolidinyl)-

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매

실험 절차

2-(N-carboxy-phenylamino)-N-(2-chloro-4-sulphamoylphenyl)-acetamide (5.0 g) was heated in acetic anhydride (20 ml) 2 hr at 80°. The anhydride was then distilled off and the residue digested with water, filtered off and further washed with water to yield 3.5 g, m.p. 241°-243° on recrystallisation from ethyl acetate.

후처리

  1. distillationThe anhydride was then distilled off
  2. filtrationthe residue digested with water, filtered off
  3. washfurther washed with water
custom
to yield 3.5 g, m.p. 241°-243°
  • customon recrystallisation from ethyl acetate
  • 출처 및 근거

    ORD 기록
    ord-1d95f692833d4a96b7f1449fc2d253fc
    출처 데이터셋
    uspto-grants-1976_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US03963706

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