Methylamine → HCID 68291727, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](Cl)=[C:8]([C:11]([NH2:13])=[O:12])[CH:7]=[N:6][N:5]2[CH:14]=1.[CH3:15][NH2:16]>>[Br:1][C:2]1[CH:3]=[C:4]2[C:9]([NH:16][CH3:15])=[C:8]([C:11]([NH2:13])=[O:12])[CH:7]=[N:6][N:5]2[CH:14]=1Participants
3
Procedure
A solution of 6-bromo-4-chloropyrrolo[1,2-b]pyridazine-3-carboxamide (Preparation 5, 200 mg, 0.733 mmol), and methylamine (0.5 mL, 8M solution in EtOH) was heated to 80° C. for 1 hr in the CEM microwave. The reaction mixture was evaporated in vacuo to give the title compound (192 mg, 98%). HPLC (condition G): retention time=0.77 min. LCMS (condition B): m/z 269.0, 271.0.
Workup
- customThe reaction mixture was evaporated in vacuo
Sources & evidence
- ORD record
- ord-51776c526aec46d284ff4f7931120647
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09221826B2
Reaction notes
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