Water → HCID 15085982, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6](=[O:11])[C:5]2=O.Cl.[NH2:14][CH2:15][C:16]([C:18]1[CH:23]=[CH:22][C:21]([C:24]2[CH:29]=[CH:28][C:27]([F:30])=[CH:26][CH:25]=2)=[CH:20][CH:19]=1)=O.[OH2:31]>>[NH2:14][C:15]1[C:16]([C:18]2[CH:23]=[CH:22][C:21]([C:24]3[CH:29]=[CH:28][C:27]([F:30])=[CH:26][CH:25]=3)=[CH:20][CH:19]=2)=[N:7][C:8]2[C:4]([C:5]=1[C:6]([OH:11])=[O:31])=[CH:3][C:2]([F:1])=[CH:10][CH:9]=2Participants
4
Procedure
A basic aqueous solution of 4.13 g of 5-fluoroisatin in water was reacted with 9.3 g of 2-amino-1-(4'-fluoro-[1,1'-biphenyl]-4-yl)-ethanone hydrochloride by the procedure described in example 20, giving 7.13 g of the desired compound as a yellow solid, mp 241°-243° C.
Sources & evidence
- ORD record
- ord-3c971df63b2c4c5390c436db9d9dcad9
- Source dataset
- uspto-grants-1990_11
- Patent number
- US04968702
Reaction notes
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