Morpholine → 3-morpholin-4-yl-5-(trifluoromethyl)benzonitrile
Reaction equation
F[C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([C:10]([F:13])([F:12])[F:11])[CH:9]=1)[C:5]#[N:6].[NH:14]1[CH2:19][CH2:18][O:17][CH2:16][CH2:15]1>>[N:14]1([C:2]2[CH:3]=[C:4]([CH:7]=[C:8]([C:10]([F:13])([F:12])[F:11])[CH:9]=2)[C:5]#[N:6])[CH2:19][CH2:18][O:17][CH2:16][CH2:15]1Participants
3
Procedure
The title compound is prepared using an analogous method as described in Example 1.1, utilising 3-fluoro-5-(trifluoromethyl)-benzonitrile (Lancaster Synthesis GmbH) and morpholine (Fluka, Buchs, Switzerland), with a reaction temperature of 105° C. for 14 hours.
Sources & evidence
- ORD record
- ord-f79f95c8c91f4548904236bddb20f433
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07655669B2
Reaction notes
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