3-Bromo-1,1,1-trifluoro-2-propanone → HCID 86703036, compound

HRID 1851193Notes

Reaction equation

HRID 1851193 reaction equation
[CH:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:14]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)=[CH:13][N:12]3C=C(C(OCC)=O)[N:23]=[C:11]3[N:10]=2)=[CH:5][CH:4]=1)=[O:2].Br[CH2:30][C:31](=O)[C:32]([F:35])([F:34])[F:33]>>[C:15]1([C:14]2[C:9]([C:6]3[CH:5]=[CH:4][C:3]([CH:1]=[O:2])=[CH:8][CH:7]=3)=[N:10][C:11]3[N:12]([CH:30]=[C:31]([C:32]([F:35])([F:34])[F:33])[N:23]=3)[CH:13]=2)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1

Participants

3

Procedure

This compound was prepared in a manner according to ethyl 7-(4-formylphenyl)-6-phenylimidazo[1,2-a]pyrimidine-2-carboxylate by using 3-bromo-1,1,1-trifluoroacetone instead of ethyl 3-bromo-2-oxopropanoate in step 5.

Workup

  1. customThis compound was prepared in a manner

Sources & evidence

ORD record
ord-af7d0595a47a4a479b11dd72a0e20cc5
Source dataset
uspto-grants-2015_02
Patent number
US08957064B2

Reaction notes

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