4-Anilino-3-nitro-5-sulphamyl-benzoic acid → 3-Amino-4-piperidino-5-sulphamyl-benzoic acid

HRID 1287745노트

반응식

HRID 1287745 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[C:11]([S:19](=[O:22])(=[O:21])[NH2:20])[C:12]=1[N:13]1[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1)[C:7]([OH:9])=[O:8])([O-])=O.N(C1C(S(=O)(=O)N)=CC(C(O)=O)=CC=1[N+]([O-])=O)C1C=CC=CC=1>>[NH2:1][C:4]1[CH:5]=[C:6]([CH:10]=[C:11]([S:19](=[O:21])(=[O:22])[NH2:20])[C:12]=1[N:13]1[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1)[C:7]([OH:9])=[O:8]

참가 물질

3

반응물 2

HCID 215060714-Anilino-3-nitro-5-sulphamyl-benzoic acidHCID 215061073-Nitro-4-piperidino-5-sulphamyl-benzoic acid

생성물 1

HCID 215061343-Amino-4-piperidino-5-sulphamyl-benzoic acid

실험 절차

By substituting 3-nitro-4-piperidino-5-sulphamyl-benzoic acid for the 4-anilino-3-nitro-5-sulphamyl-benzoic acid of Example 9 B, the above compound was obtained with a melting point of 279° C (decomp.) after recrystallization from aqueous methanol.

후처리

  1. customthe above compound was obtained with a melting point of 279° C (decomp.)
  2. customafter recrystallization from aqueous methanol

출처 및 근거

ORD 기록
ord-0575dff72e2b47b48399debe67cea41d
출처 데이터셋
uspto-grants-1976_10
특허 번호
US03985777

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