Cyclobutylamine → HCID 22734150, compound
Reaction equation
[CH3:1][O:2][C:3]1[C:11]2[O:10][C:9]([C:12]([OH:14])=O)=[CH:8][C:7]=2[CH:6]=[CH:5][CH:4]=1.[CH:15]1([NH2:19])[CH2:18][CH2:17][CH2:16]1>>[CH:15]1([NH:19][C:12]([C:9]2[O:10][C:11]3[C:3]([O:2][CH3:1])=[CH:4][CH:5]=[CH:6][C:7]=3[CH:8]=2)=[O:14])[CH2:18][CH2:17][CH2:16]1Participants
3
Procedure
Substantially the same procedure as in Example 219 was repeated using a starting material, 7-methoxybenzofuran-2-carboxylic acid, and cyclobutylamine to give N-Cyclobutyl-7-methoxybenzofuran-2-carboxamide (Compound 289a). Successively, it was formylated to give N-cyclobutyl-4-formyl-7-methoxybenzofuran-2-carboxamide (Compound 289b), then compound 289b was reacted with methylamine hydrochloride to give Compound 289 as a white solid.
Sources & evidence
- ORD record
- ord-b917a2fb409a4298a49cd8404bd8257e
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06716987B1
Reaction notes
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