HCID 13910471, compound → HCID 13910488, compound

HRID 2118620Notes

Reaction equation

HRID 2118620 reaction equation
[C:1]([NH:9][C:10]([N:12]1[C:20]2[C:15](=[CH:16][C:17](C)=[CH:18][CH:19]=2)[CH2:14][C:13]1=[O:22])=[O:11])(=[O:8])[C:2]1[CH:7]=CC=C[CH:3]=1.[C:23](NC(N1C2C(=CC(C)=CC=2)CC1=O)=O)(=O)C.C(NC(N1C2C(=CC(C)=CC=2)CC1=O)=O)(=O)C(C)(C)C.C(NC(N1C2C(=CC(C)=CC=2)CC1=O)=O)(=O)CC.C(NC(N1C2C(=CC(OC)=CC=2)CC1=O)=O)(=O)CCC.C(NC(N1C2C(=CC(OC)=CC=2)CC1=O)=O)(=O)C1C=CC=CC=1.C(NC(N1C2C(=CC(OC)=CC=2)CC1=O)=O)(=O)C>>[C:1]([NH:9][C:10]([N:12]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH2:14][C:13]1=[O:22])=[O:11])(=[O:8])[C:2]([CH3:3])([CH3:7])[CH3:23]

Participants

8

Procedure

Employing the above procedure, 1-(N-benzoylcarbamoyl)-5-methyloxindole, 1-(N-acetylcarbamoyl)-5-methyloxindole, 1-(N-pivaloylcarbamoyl)-5-methyloxindole, 1-(N-propionylcarbamoyl)-5-methyloxindole, 1-(N-butyrylcarbamoyl)-5-methoxyoxindole, 1-(N-benzoylcarbamoyl)-5-methoxyoxindole and 1-(N-acetylcarbamoyl)-5-methoxyoxindole are prepared.

Workup

  1. customare prepared

Sources & evidence

ORD record
ord-4c557ce58d5b4cba8ea78892b28f04d5
Source dataset
uspto-grants-1987_07
Patent number
US04678802

Reaction notes

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