Methylamine → HCID 15016287, compound
Reaction equation
[C:1]([CH:4]([O:6][C:7]1[N:11]=[CH:10][N:9]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([C:18]([F:21])([F:20])[F:19])[CH:13]=2)[N:8]=1)[CH3:5])([OH:3])=O.[C:22](N1C=CN=C1)([N:24]1C=CN=C1)=O.CN>>[CH3:22][NH:24][C:1]([CH:4]([O:6][C:7]1[N:11]=[CH:10][N:9]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([C:18]([F:21])([F:20])[F:19])[CH:13]=2)[N:8]=1)[CH3:5])=[O:3]Participants
4
Procedure
The process was carried out as was Example 45, starting with 3 g of the compound of Example 24, 3.4 g of carbonyldiimidazole and 3 ml of 40% aqueous methylamine. The product was not recrystallized, and amounted to 2.7 g of the desired product, m.p. 137°-139°.
Workup
- customThe product was not recrystallized
Sources & evidence
- ORD record
- ord-3e8cd3d7a611494ea054f8f2fe60d7ea
- Source dataset
- uspto-grants-1990_06
- Patent number
- US04931083
Reaction notes
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