Methylamine → HCID 13136976, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]2[C:9]3[CH2:14][CH2:13][N:12]([CH2:15][C:16](=O)[CH3:17])[CH2:11][C:10]=3[C:19](=[O:21])[O:20][C:5]=2[CH:4]=1.[CH3:22][NH2:23]>>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]2[C:9]3[CH2:14][CH2:13][N:12]([CH2:15][CH:16]([NH:23][CH3:22])[CH3:17])[CH2:11][C:10]=3[C:19](=[O:21])[O:20][C:5]=2[CH:4]=1Participants
3
Procedure
Prepared by the method described for Example 51 from 1,2,3,4-tetrahydro-8-methoxy-3-(2-oxopropyl)-5H-[1]benzopyrano[3,4-c]pyridin-5-one (16.5 g, 0.057 moles) and methylamine (8 ml, 0.18 moles). Recrystallization from ethyl acetate gave the product (12.0 g), mp 109°-111° C.
Workup
- customPrepared by the method
- customRecrystallization from ethyl acetate
Sources & evidence
- ORD record
- ord-4e35a1afc79e43138a241a9942e784c4
- Source dataset
- uspto-grants-1983_05
- Patent number
- US04382939
Reaction notes
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