Hydrochloric Acid → HCID 23356470, compound
Reaction equation
[C:1]([C:3]1[N:7]2[CH:8]=[CH:9][N:10]=[C:11]([CH3:12])[C:6]2=[CH:5][CH:4]=1)#[N:2].Cl.[OH2:14]>>[C:1]([C:3]1[N:7]2[CH:8]=[CH:9][N:10]=[C:11]([CH3:12])[C:6]2=[CH:5][CH:4]=1)(=[O:14])[NH2:2]Participants
4
Procedure
To 2.0 g of 6-cyano-1-methylpyrrolo[1,2-a]pyrazine prepared in Preparation Example 4 were added 10 ml of water and 5 ml of hydrochloric acid; and the reaction mixture was reacted at 80° C. for 2 hours, cooled to room temperature, extracted with ethyl acetate, and concentrated. The residue was chromatographed over silica gel to obtain 1.0 g of title compound.
Workup
- customand the reaction mixture was reacted at 80° C. for 2 hours
- extractionextracted with ethyl acetate
- concentrationconcentrated
- customThe residue was chromatographed over silica gel
Sources & evidence
- ORD record
- ord-4b28ef071c2f4c99be7f5b44da0e7b60
- Source dataset
- uspto-grants-1997_01
- Patent number
- US05593984
Reaction notes
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