5-Chloromethyloxazolidin-2-one → HCID 18401718, compound
Reaction equation
[F:1][C:2]([F:34])([F:33])[C:3]1[CH:4]=[C:5]([CH:26]=[C:27]([C:29]([F:32])([F:31])[F:30])[CH:28]=1)[C:6]([N:8]1[CH2:25][CH2:24][C:11]2([N:15]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=3[Cl:22])[CH2:14][NH:13][C:12]2=[O:23])[CH2:10][CH2:9]1)=[O:7].Cl[CH2:36][CH:37]1[O:41][C:40](=[O:42])[NH:39][CH2:38]1>>[F:32][C:29]([F:31])([F:30])[C:27]1[CH:26]=[C:5]([CH:4]=[C:3]([C:2]([F:1])([F:33])[F:34])[CH:28]=1)[C:6]([N:8]1[CH2:9][CH2:10][C:11]2([N:15]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=3[Cl:22])[CH2:14][N:13]([CH2:36][CH:37]3[O:41][C:40](=[O:42])[NH:39][CH2:38]3)[C:12]2=[O:23])[CH2:24][CH2:25]1)=[O:7]Participants
3
Procedure
The title compound, MS: m/e=604.9 (M+H+), was prepared in accordance with the general method of example 71 from 8-(3,5-bis-trifluoromethyl-benzoyl)-1-(2-chloro-phenyl)-1,3,8-triaza-spiro[4.5]decan-4-one and 5-chloromethyl-2-oxazolidinone.
Sources & evidence
- ORD record
- ord-0b5f94e9c9e1413e83875532f33a1382
- Source dataset
- uspto-grants-2002_11
- Patent number
- US06482829B2
Reaction notes
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