3,5-Dichloro-3-(2-methoxyphenyl)indolin-2-one → HCID 67429904, compound

HRID 1662655Notes

Reaction equation

HRID 1662655 reaction equation
Cl[C:2]1([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=2[O:19][CH3:20])[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([Cl:11])[CH:9]=2)[NH:4][C:3]1=[O:12].FC(F)(F)C(O)=O.[NH2:28][C@@H:29]([CH2:35][C:36]([NH2:38])=[O:37])[C:30]([N:32]([CH3:34])[CH3:33])=[O:31]>>[Cl:11][C:8]1[CH:9]=[C:10]2[C:5](=[CH:6][CH:7]=1)[NH:4][C:3](=[O:12])[C:2]2([NH:28][C@@H:29]([CH2:35][C:36]([NH2:38])=[O:37])[C:30]([N:32]([CH3:34])[CH3:33])=[O:31])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[O:19][CH3:20]

Participants

3

Reactant 2

HCID 219059133,5-Dichloro-3-(2-methoxyphenyl)indolin-2-oneHCID 86625690HCID 86625690, compound

Product 1

HCID 67429904HCID 67429904, compound

Procedure

With 1.08 g of 3,5-dichloro-3-(2-methoxyphenyl)-1,3-dihydro-2H-indol-2-one and the compound obtained in Step 67-2 (15.5 mmol, crude form) as starting materials, 576 mg of the title compound (colorless amorphous) was obtained by a similar method to Step 4-2.

Sources & evidence

ORD record
ord-ba75dbd2e8e24a659a93fb3c5a445131
Source dataset
uspto-grants-2011_10
Patent number
US08030499B2

Reaction notes

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