Methylamine → HCID 15016290, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH:12]=[N:11][C:10]([O:13][CH:14]([C:16]([OH:18])=O)[CH3:15])=[N:9]2)=[CH:4][CH:3]=1.[C:19](N1C=CN=C1)([N:21]1C=CN=C1)=O.CN>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[CH:12]=[N:11][C:10]([O:13][CH:14]([C:16]([NH:21][CH3:19])=[O:18])[CH3:15])=[N:9]2)=[CH:6][CH:7]=1Participants
4
Procedure
The process was carried out as was Example 45, starting with 3 g of the compound of Example 37, 2.3 g of carbonyldiimidazole and 2 ml of 40% aqueous methylamine. The product was recrystallized from ethanol to obtain 2.5 g of the desired product, m.p. 176°-178°.
Workup
- customThe product was recrystallized from ethanol
Sources & evidence
- ORD record
- ord-1c3c0def01f140038baf2f0f65dc3282
- Source dataset
- uspto-grants-1990_06
- Patent number
- US04931083
Reaction notes
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