5-(Bromomethyl)thiophene-2-carbonitrile → HCID 11697599, compound
Reaction equation
CO[C:3](=[O:12])[C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][C:5]=1[F:11].Br[CH2:14][C:15]1[S:19][C:18]([C:20]#[N:21])=[CH:17][CH:16]=1.[CH3:22][C@@H:23]1[CH2:27][CH2:26][CH2:25][N:24]1[CH2:28][C@@H:29]1[CH2:33][CH2:32][CH2:31][NH:30]1>>[F:11][C:5]1[CH:6]=[C:7]([CH:8]=[CH:9][C:4]=1[C:3]([N:30]1[CH2:31][CH2:32][CH2:33][C@H:29]1[CH2:28][N:24]1[CH2:25][CH2:26][CH2:27][C@H:23]1[CH3:22])=[O:12])[O:10][CH2:14][C:15]1[S:19][C:18]([C:20]#[N:21])=[CH:17][CH:16]=1Participants
4
Procedure
The title compound is prepared in a manner substantially analogous to Procedures D and E using 2-fluoro-4-hydroxy-benzoic acid methyl ester [CAS 197507-22-5], 5-bromomethyl-thiophene-2-carbonitrile [CAS 134135-41-4], and 2-(R)-methyl-1-(2-(S)-pyrrolidinylmethyl)pyrrolidine. MS (ES+) m/e 428.3
Sources & evidence
- ORD record
- ord-0b95d970eb3c48ce981ad54ffdee82e0
- Source dataset
- uspto-grants-2010_12
- Patent number
- US07846950B2
Reaction notes
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