Pyrrolidine → HCID 24809925, compound
Reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[O:14][N:13]=[CH:12][C:11]=2[C:15]([OH:17])=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].[NH:18]1[CH2:22][CH2:21][CH2:20][CH2:19]1>>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([C:10]2[O:14][N:13]=[CH:12][C:11]=2[C:15]([N:18]2[CH2:22][CH2:21][CH2:20][CH2:19]2)=[O:17])=[CH:8][CH:9]=1)([O-:3])=[O:2]Participants
3
Procedure
The title compound was prepared from 5-(4-nitrophenyl)isoxazole-4-carboxylic acid (11.7 mg, 0.050 mmol) and pyrrolidine (4.3 mg, 0.060 mmol) as described in synthetic method A and thereafter purified, first by preparative HPLC method A and then by method B, to give a solid (13.4 mg). MS (pos) m/z 288.2 (M+H).
Workup
- custompurified, first by preparative HPLC method A
Sources & evidence
- ORD record
- ord-0a858d63f8ee41e7ab79a7a25c461986
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07666888B2
Reaction notes
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