HCID 20194063, compound → HCID 13922148, compound

HRID 2118618Notes

Reaction equation

HRID 2118618 reaction equation
[C:1]([NH:4][C:5]([N:7]1[C:15]2[C:10](=[CH:11][C:12]([C:16](=[O:18])[CH3:17])=[CH:13][CH:14]=2)[CH2:9][C:8]1=[O:19])=[O:6])(=[O:3])[CH3:2].C(NC(N1C2[C:32](=[CH:33][C:34](C(=O)C)=CC=2)[CH2:31][C:30]1=O)=O)(=O)C(C)(C)C.C(NC(N1C2C(=CC(C(=O)C)=CC=2)CC1=O)=O)(=O)CC>>[C:1]([NH:4][C:5]([N:7]1[C:15]2[C:10](=[CH:11][C:12]([C:16](=[O:18])[CH3:17])=[CH:13][CH:14]=2)[CH2:9][C:8]1=[O:19])=[O:6])(=[O:3])[C:2]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1

Participants

4

Reactant 3

HCID 20194063HCID 20194063, compoundHCID 20194064HCID 20194064, compoundHCID 20194067HCID 20194067, compound

Product 1

HCID 13922148HCID 13922148, compound

Procedure

In a similar manner 1-(N-acetylcarbamoyl)-5-acetyloxindole, 1-(N-s-butyrylcarbamoyl)-5-acetyloxindole, 1-(N-pivaloylcarbamoyl)-5-acetyloxindole and 1-(N-propionylcarbamoyl)-5-acetyloxindole are prepared.

Sources & evidence

ORD record
ord-8181086f71204e718e2ebc37739eade0
Source dataset
uspto-grants-1987_07
Patent number
US04678802

Reaction notes

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