Pyrrolidine → HCID 69308874, compound

HRID 2250614Notes

Reaction equation

HRID 2250614 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

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

  1. customThe mixture was partitioned between ethyl acetate (20 mL) and 1N hydrochloric acid (10 mL)
  2. washThe organic layer was washed with water (10 mL) three times, saturated sodium bicarbonate (10 mL), and brine
  3. customdried
  4. customevaporated

Sources & evidence

ORD record
ord-64840302822147678c70b10ce6c48038
Source dataset
uspto-grants-2008_01
Patent number
US07317009B2

Reaction notes

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