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Potassium Carbonate → 6-[(4"-Aminobenzoyl)azo]-8-{[(aminocarbonyl)oxy]methyl}-4,7-dihydroxy-1,1a,2,8,8a,8b-hexahydro-8a-methoxy-5-methyl-azirino[2',3':3,4]pyrrolo[1,2-a)indole

HRID 414220
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HRID 414220 반응식
[CH3:1][C:2]1[C:8](=[O:9])[C:7]2[N:10]3[C@@:14]([O:21][CH3:22])([C@H:15]([CH2:16][O:17][C:18]([NH2:20])=[O:19])[C:6]=2[C:4](=[O:5])[C:3]=1OC)[C@H:13]1[NH:23][C@H:12]1[CH2:11]3.[NH2:26][C:27]1[CH:36]=[CH:35][C:30]([C:31]([NH:33][NH2:34])=[O:32])=[CH:29][CH:28]=1.C(=O)([O-])[O-].[K+].[K+]>>[NH2:26][C:27]1[CH:36]=[CH:35][C:30]([C:31]([N:33]=[N:34][C:3]2[C:2]([CH3:1])=[C:8]([OH:9])[C:7]3[N:10]4[CH2:11][CH:12]5[NH:23][CH:13]5[C:14]4([O:21][CH3:22])[CH:15]([CH2:16][O:17][C:18]([NH2:20])=[O:19])[C:6]=3[C:4]=2[OH:5])=[O:32])=[CH:29][CH:28]=1
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 11430Potassium CarbonateHCID 19972Mitomycin AHCID 214504-Aminobenzoic acid hydrazide

생성물 1

HCID 1363428356-[(4"-Aminobenzoyl)azo]-8-{[(aminocarbonyl)oxy]methyl}-4,7-dihydroxy-1,1a,2,8,8a,8b-hexahydro-8a-methoxy-5-methyl-azirino[2',3':3,4]pyrrolo[1,2-a)indole수율 40.5%

실험 절차

In a similar manner to that described in Example 17, mitomycin A (302 mg), 4-aminobenzoylhydrazine (389 mg) and potassium carbonate (150 mg) are used to obtain the desired product (163 mg) with a yield of 40.5%.

출처 및 근거

ORD 기록
ord-f43c1da2a11c473abcc24aaa81d56c1c
출처 데이터셋
uspto-grants-1988_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04791113

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