Cyclopropylamine → HCID 178471857, compound
Reaction equation
[Cl:1][C:2]1[C:3]([F:23])=[C:4]([C:17]([CH3:22])=[C:18]([F:21])[C:19]=1[F:20])[C:5]([C:7](=[CH:13]OCC)[C:8]([O:10][CH2:11][CH3:12])=[O:9])=[O:6].[CH:24]1([NH2:27])[CH2:26][CH2:25]1>>[Cl:1][C:2]1[C:3]([F:23])=[C:4]([C:17]([CH3:22])=[C:18]([F:21])[C:19]=1[F:20])[C:5]([C:7](=[CH:13][NH:27][CH:24]1[CH2:26][CH2:25]1)[C:8]([O:10][CH2:11][CH3:12])=[O:9])=[O:6]Participants
3
Procedure
Employing ethyl 2-(3-chloro-2,4,5-trifluoro-6-methylbenzoyl)-3-ethoxyacrylate (360 mg) and cyclopropylamine (60 mg), the procedure of Reference Example 21 is repeated to give ethyl 2-(3-chloro-2,4,5-trifluoro-6-methylbenzoyl)-3-cyclopropylaminoacrylate (410 mg), as brown oil.
Sources & evidence
- ORD record
- ord-7e7857bc6f7d4018b16125e815d1dcf2
- Source dataset
- uspto-grants-1997_01
- Patent number
- US05591744
Reaction notes
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