Nitrogen → HCID 66953366, compound
Reaction equation
[CH3:1][O:2][C:3]([C:5]1[N:6]=[C:7]2[C:22](I)=[CH:21][C:20]([N:24]3[CH2:29][CH2:28][O:27][CH2:26][CH2:25]3)=[CH:19][N:8]2[C:9](=[O:18])[C:10]=1[CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[O:4].[CH:30]([O:32][CH2:33][CH2:34][CH2:35][CH3:36])=[CH2:31].N#N.O>CN(C=O)C.CC([O-])=O.CC([O-])=O.[Pd+2].C1(P(C2C=CC=CC=2)CCCP(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[CH3:1][O:2][C:3]([C:5]1[N:6]=[C:7]2[C:22]([C:30]([O:32][CH2:33][CH2:34][CH2:35][CH3:36])=[CH2:31])=[CH:21][C:20]([N:24]3[CH2:29][CH2:28][O:27][CH2:26][CH2:25]3)=[CH:19][N:8]2[C:9](=[O:18])[C:10]=1[CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[O:4]Participants
8
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
3-Benzyl-9-iodo-7-morpholin-4-yl-4-oxo-4H-pyrido[1,2-a]pyrimidine-2-carboxylic acid methyl ester (1 g, 1.92 mmol), n-Butyl vinyl ether (961 mg, 9.59 mmol), 1,3-Bis(diphenylphosphino)propane (DPPP) (24 mg, 0.058 mmol), Pd(OAc)2 (11 mg, 0.048 mmol) were mixed in DMF (15 ml). The mixture was heated at 80° C. under the atmosphere of N2 overnight, after which water was added and then extracted with dichloromethane. The extracts were combined, washed with brine, dried over sodium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography to give the desired product (540 mg, yield 54%).
Workup
- extractionextracted with dichloromethane
- washwashed with brine
- dry with materialdried over sodium sulfate
- customevaporated under reduced pressure
- customThe residue was purified by column chromatography
Sources & evidence
- ORD record
- ord-71aaaefa3cf94288a2a561d1cba2e084
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08563562B2
Reaction notes
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