Pyrrolidine → HCID 70009270, compound
Reaction equation
Cl[CH:2]([C:10]1[CH:15]=[CH:14][C:13]([C:16]2[N:21]3[CH2:22][CH2:23][C:24]4[NH:25][C:26](=[O:29])[CH:27]=[CH:28][C:19]([C:20]=43)=[CH:18][N:17]=2)=[CH:12][CH:11]=1)[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[NH:30]1[CH2:34][CH2:33][CH2:32][CH2:31]1>C(Cl)(Cl)Cl>[C:4]1([CH2:3][CH:2]([C:10]2[CH:15]=[CH:14][C:13]([C:16]3[N:21]4[CH2:22][CH2:23][C:24]5[NH:25][C:26](=[O:29])[CH:27]=[CH:28][C:19]([C:20]=54)=[CH:18][N:17]=3)=[CH:12][CH:11]=2)[N:30]2[CH2:34][CH2:33][CH2:32][CH2:31]2)[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
This compound was prepared from intermediate 247b and pyrrolidine according to the procedure described in Example 245, with the exception of chloroform as solvent. Received 40 mg (11%).
Sources & evidence
- ORD record
- ord-335f30528bd9402d849f8402e080c7ce
- Source dataset
- uspto-grants-2003_04
- Patent number
- US06548494B1
Reaction notes
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