Pyrrolidine → HCID 69308874, compound
Reaction equation
[C:1]([C:3]1[CH:4]=[C:5]([C:9]2[C:10]3[N:11]([C:22]([CH2:25][CH3:26])=[CH:23][CH:24]=3)[N:12]=[C:13]([C:19]([OH:21])=O)[C:14]=2[S:15]([CH3:18])(=[O:17])=[O:16])[CH:6]=[CH:7][CH:8]=1)#[N:2].[NH:27]1[CH2:31][CH2:30][CH2:29][CH2:28]1.Cl.CN(C)CCCN=C=NCC.ON1C2C=CC=CC=2N=N1>CN(C)C=O>[CH2:25]([C:22]1[N:11]2[N:12]=[C:13]([C:19]([N:27]3[CH2:31][CH2:30][CH2:29][CH2:28]3)=[O:21])[C:14]([S:15]([CH3:18])(=[O:17])=[O:16])=[C:9]([C:5]3[CH:4]=[C:3]([CH:8]=[CH:7][CH:6]=3)[C:1]#[N:2])[C:10]2=[CH:24][CH:23]=1)[CH3:26]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 4-(3-cyanophenyl)-7-ethyl-3-(methylsulfonyl)pyrrolo[1,2-b]pyridazine-2-carboxylic acid (40.0 mg), pyrrolidine (10.8 mg), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (31.1 mg), and 1-hydroxybenzotriazole (21.9 mg) in N,N-dimethylformamide (1 mL) was stirred for 6 hour at room temperature. The mixture was partitioned between ethyl acetate (20 mL) and 1N hydrochloric acid (10 mL). The organic layer was washed with water (10 mL) three times, saturated sodium bicarbonate (10 mL), and brine, dried, and evaporated to give 3-[7-ethyl-3-(methylsulfonyl)-2-(1-pyrrolidinylcarbonyl)pyrrolo[1,2-b]pyridazin-4-yl]benzonitrile as an yellow solid (35.6 mg).
Workup
- customThe mixture was partitioned between ethyl acetate (20 mL) and 1N hydrochloric acid (10 mL)
- washThe organic layer was washed with water (10 mL) three times, saturated sodium bicarbonate (10 mL), and brine
- customdried
- customevaporated
Sources & evidence
- ORD record
- ord-64840302822147678c70b10ce6c48038
- Source dataset
- uspto-grants-2008_01
- Patent number
- US07317009B2
Reaction notes
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