Ethanolamine → HCID 69309298, compound
Reaction equation
[CH2:1]([C:3]1[N:7]2[N:8]=[C:9]([CH3:22])[C:10]([C:19]([OH:21])=O)=[C:11]([C:12]3[CH:13]=[N:14][CH:15]=[C:16]([CH3:18])[CH:17]=3)[C:6]2=[CH:5][CH:4]=1)[CH3:2].Cl.C(N=C=NCCCN(C)C)C.[NH2:35][CH2:36][CH2:37][OH:38]>CN(C)C=O>[CH2:1]([C:3]1[N:7]2[N:8]=[C:9]([CH3:22])[C:10]([C:19]([NH:35][CH2:36][CH2:37][OH:38])=[O:21])=[C:11]([C:12]3[CH:13]=[N:14][CH:15]=[C:16]([CH3:18])[CH:17]=3)[C:6]2=[CH:5][CH:4]=1)[CH3:2]Participants
Procedure
To a solution of 7-ethyl-2-methyl-4-(5-methyl-3-pyridinyl)pyrrolo[1,2-b]pyridazine-3-carboxylic acid (70 mg), 1-ethyl-3-(3′-dimethylaminopropyl)carbodiimide hydrochloride (68.2 mg) and 1-hydroxybenotriazole (48 mg) in dimethylformamide (2 mL) was added 2-aminoethanol (17.4 mg) and the mixture was stirred at ambient temperature for 1 hour. The mixture was partitioned between ethyl acetate and water. The organic layer was separated, washed with saturated sodium bicarbonate solution, water and brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was purified by silica gel column chromatography eluting with a mixture of chloroform and methanol (50:1–10:1). The crude product was triturated with isopropylether to give 7-ethyl-N-(2-hydroxyethyl)-2-methyl-4-(5-methyl-3-pyridinyl)pyrrolo[1,2-b]pyridazine-3-carboxamide as a yellow powder (47 mg).
Workup
- customThe mixture was partitioned between ethyl acetate and water
- customThe organic layer was separated
- washwashed with saturated sodium bicarbonate solution, water and brine
- dry with materialdried over magnesium sulfate
- customevaporated in vacuo
- customThe residue was purified by silica gel column chromatography
- washeluting with a mixture of chloroform and methanol (50:1–10:1)
- customThe crude product was triturated with isopropylether
Sources & evidence
- ORD record
- ord-76ab76da8bc34c108f62725f1b4dc655
- Source dataset
- uspto-grants-2006_12
- Patent number
- US07153854B2
Reaction notes
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