Pyrrolidine → HCID 59152279, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]=[C:10]([S:13][CH2:14][C:15]([OH:17])=O)[S:11][CH:12]=2)=[CH:4][CH:3]=1.[NH:18]1[CH2:22][CH2:21][CH2:20][CH2:19]1>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[N:9]=[C:10]([S:13][CH2:14][C:15]([N:18]3[CH2:22][CH2:21][CH2:20][CH2:19]3)=[O:17])[S:11][CH:12]=2)=[CH:6][CH:7]=1Participants
3
Procedure
The title compound was prepared analogously as described in Example 30(d) from 100 mg (0.37 mmol) of [4-(4-fluoro-phenyl)-thiazol-2-ylsulfanyl]-acetic acid and 52.8 mg (0.74 mmol) of pyrrolidine. Yield: 17 mg.
Sources & evidence
- ORD record
- ord-dbb8cfdef3bb4645a7a1823dd2f97982
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08188291B2
Reaction notes
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