HCID 86694554, compound → HCID 86694555, compound

HRID 714580Notes

Reaction equation

HRID 714580 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([NH:9][C:10]2[C:19]3[C:14](=[CH:15][C:16](F)=[C:17]([N+:20]([O-:22])=[O:21])[CH:18]=3)[N:13]=[CH:12][C:11]=2[C:24]#[N:25])[CH:5]=[CH:6][C:7]=1[F:8].[OH:26][C:27]1[CH:32]=[CH:31][N:30]=[CH:29][CH:28]=1>>[Cl:1][C:2]1[CH:3]=[C:4]([NH:9][C:10]2[C:19]3[C:14](=[CH:15][C:16]([O:26][C:27]4[CH:32]=[CH:31][N:30]=[CH:29][CH:28]=4)=[C:17]([N+:20]([O-:22])=[O:21])[CH:18]=3)[N:13]=[CH:12][C:11]=2[C:24]#[N:25])[CH:5]=[CH:6][C:7]=1[F:8]

Participants

3

Reactant 2

HCID 86694554HCID 86694554, compoundHCID 178418642HCID 178418642, compound

Product 1

HCID 86694555HCID 86694555, compound

Procedure

The compound was prepared according to the process of Preparation 2 and with 4-(3-chloro-4-fluorophenylamino)-7-fluoro-6-nitroquinoline-3-carbonitrile and 4-hydroxypyridine as starting materials.

Workup

  1. customThe compound was prepared

Sources & evidence

ORD record
ord-3ae960a487c64e1794dde82864207302
Source dataset
uspto-grants-2015_11
Patent number
US09187458B2

Reaction notes

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