1187917-12-9 → HCID 44230317, compound

HRID 1949295Notes

Reaction equation

HRID 1949295 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:12]([C:13]3[CH:18]=[CH:17][CH:16]=[C:15]([C:19]([F:22])([F:21])[F:20])[CH:14]=3)=[CH:11][C:10]([C:23]([OH:25])=O)=[N:9]2)=[CH:4][CH:3]=1.ClC1C=C(N2C(C3C=C(F)C=C(Cl)C=3)=CC(C([N:49]3[CH2:53][C:52](=[O:54])[NH:51][CH2:50]3)=O)=N2)C=CC=1F>>[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:12]([C:13]3[CH:18]=[CH:17][CH:16]=[C:15]([C:19]([F:20])([F:21])[F:22])[CH:14]=3)=[CH:11][C:10]([C:23]([N:49]3[CH2:53][C:52](=[O:54])[NH:51][CH2:50]3)=[O:25])=[N:9]2)=[CH:4][CH:3]=1

Participants

3

Procedure

The preparation of the title compound takes place starting from the compound of Example 87A in analogy to the synthesis of the compound of Example 1. 28 mg (74% of theory) of the title compound are obtained.

Sources & evidence

ORD record
ord-3a2ba18a6716411286ca6a33ce123ee4
Source dataset
uspto-grants-2013_03
Patent number
US08399682B2

Reaction notes

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