6-Benzoyl-1,3-dihydro-2H-indol-2-one → HCID 13770527, compound

HRID 236373Notes

Reaction equation

HRID 236373 reaction equation
C(C1C=C2C(CC(=O)N2)=CC=1)(=O)C1C=CC=CC=1.CN1C2C(=CC=C(C(=O)C3C=CC=CC=3)C=2)CC1=O.[CH2:38]([N:41]1[C:49]2[C:44](=[CH:45][CH:46]=[C:47]([C:50](=[O:57])[C:51]3[CH:56]=[CH:55][CH:54]=[CH:53][CH:52]=3)[CH:48]=2)[CH2:43][C:42]1=[O:58])[CH2:39]C.C(N1C2C(=CC=C(C(=O)C3C=CC=CC=3)C=2)CC1=O)(C)C>>[CH2:38]([N:41]1[C:49]2[C:44](=[CH:45][CH:46]=[C:47]([C:50](=[O:57])[C:51]3[CH:56]=[CH:55][CH:54]=[CH:53][CH:52]=3)[CH:48]=2)[CH2:43][C:42]1=[O:58])[CH3:39]

Participants

5

Reactant 4

HCID 134082316-Benzoyl-1,3-dihydro-2H-indol-2-oneHCID 20189441HCID 20189441, compoundHCID 20189447HCID 20189447, compoundHCID 20189453HCID 20189453, compound

Product 1

HCID 13770527HCID 13770527, compound

Procedure

Starting with 6-benzoyloxindole and the appropriate dialkyl sulfate and employing the procedure of Preparation G6, 1-methyl-6-benzoyloxindole, 1-n-propyl-6-benzoyloxindole and 1-i-propyl-6-benzoyloxindole are prepared.

Workup

  1. customare prepared

Sources & evidence

ORD record
ord-3618efe7038e41bf81d47b17a8480b16
Source dataset
uspto-grants-1987_02
Patent number
US04644005

Reaction notes

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