HCID 18614821, compound → HCID 178517261, compound

HRID 1637930Notes

Reaction equation

HRID 1637930 reaction equation
[N:1]1([CH2:6][C:7]2[CH:13]=[CH:12][C:10]([NH2:11])=[CH:9][CH:8]=2)[CH2:5][CH:4]=[CH:3][CH2:2]1.C(O[C:17](=[C:24]1[C:32]2[C:27](=[CH:28][CH:29]=[C:30]([N+:33]([O-:35])=[O:34])[CH:31]=2)[NH:26][C:25]1=[O:36])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)C>CN(C=O)C>[N:1]1([CH2:6][C:7]2[CH:13]=[CH:12][C:10]([NH:11]/[C:17](=[C:24]3\[C:25](=[O:36])[NH:26][C:27]4[C:32]\3=[CH:31][C:30]([N+:33]([O-:35])=[O:34])=[CH:29][CH:28]=4)/[C:18]3[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=3)=[CH:9][CH:8]=2)[CH2:5][CH:4]=[CH:3][CH2:2]1

Participants

4

Procedure

Prepared from 4-(2,5-dihydro-pyrrol-1-ylmethyl)aniline and 3-(1-ethoxy-1-phenylmethylidene)-5-nitro-2-indolinone in DMF.

Sources & evidence

ORD record
ord-7c7e2a9dfa32485584a19ab2867b22e7
Source dataset
uspto-grants-2000_03
Patent number
US06043254

Reaction notes

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