Trifluoroacetic anhydride → HCID 86606175, compound

HRID 2243821Notes

Reaction equation

HRID 2243821 reaction equation
[N:1]12[CH2:9][CH2:8][CH:5]([CH2:6][CH2:7]1)[N:4]([C:10]([C:12]1[O:13][C:14]([C:17]3[CH:22]=[CH:21][C:20]([NH2:23])=[CH:19][CH:18]=3)=[CH:15][CH:16]=1)=[O:11])[CH2:3][CH2:2]2.[F:24][C:25]([F:36])([F:35])[C:26]([O:28][C:29](=[O:34])[C:30]([F:33])([F:32])[F:31])=[O:27]>>[F:24][C:25]([F:36])([F:35])[C:26]([OH:28])=[O:27].[N:1]12[CH2:7][CH2:6][CH:5]([CH2:8][CH2:9]1)[N:4]([C:10]([C:12]1[O:13][C:14]([C:17]3[CH:22]=[CH:21][C:20]([NH:23][C:29](=[O:34])[C:30]([F:31])([F:32])[F:33])=[CH:19][CH:18]=3)=[CH:15][CH:16]=1)=[O:11])[CH2:3][CH2:2]2

Participants

3

Reactant 2

HCID 9845Trifluoroacetic anhydrideHCID 10425586HCID 10425586, compound

Product 1

HCID 86606175HCID 86606175, compound

Procedure

The title compound was prepared according to Method D from (1,4-diaza-bicyclo[3.2.2]non-4-yl)-5-(4-aminophenyl)-furan-2-yl-methanone and trifluoroacetic anhydride. Mp. 219° C.

Sources & evidence

ORD record
ord-f2a9675ffc314ee7a337bfca22104773
Source dataset
uspto-grants-2010_03
Patent number
US07678788B2

Reaction notes

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