Pyridine → HCID 69001486, compound
Reaction equation
[NH2:1][C:2]1[C:7]([C:8]#[N:9])=[C:6]2[O:10][CH2:11][O:12][C:5]2=[CH:4][C:3]=1[C:13]1[O:14][C:15]2[C:20]([CH2:21][CH:22]=1)=[CH:19][CH:18]=[C:17]([N:23]([CH3:25])[CH3:24])[CH:16]=2.N1C=CC=CC=1.[CH2:32]([O:34][C:35](Cl)=[O:36])[CH3:33].CCCCCC.[CH3:44][CH2:45][O:46][C:47](C)=[O:48]>C(Cl)Cl>[C:8]([C:7]1[C:2]([N:1]([C:47]([O:46][CH2:45][CH3:44])=[O:48])[C:35]([O:34][CH2:32][CH3:33])=[O:36])=[C:3]([C:13]2[O:14][C:15]3[C:20]([CH2:21][CH:22]=2)=[CH:19][CH:18]=[C:17]([N:23]([CH3:25])[CH3:24])[CH:16]=3)[CH:4]=[C:5]2[O:12][CH2:11][O:10][C:6]=12)#[N:9]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 2-amino-3-cyano-7-dimethylamino-4-(methylenedioxy)phenyl-4H-chromene (53 mg, 0.16 mmol) in methylenechloride (3 ml) was added pyridine (0.06 ml, 0.74 mmol), followed by ethylchloroformate (0.045 ml, 0.47 mmol). The mixture was stirred at room temperature overnight, then diluted with 1:1 hexane/EtOAc (45 ml), washed with water, 2N HCl, water and brine. The organic phase was dried over sodium sulfate and concentrated in vacuo. The residue was purified by chromatography (3:1 hexane/EtOAc) to yield the title compound as a yellow solid (5 mg, 7%). 1H NMR (CDCl3): 6.84-6.61 (m, 4H), 6.49-6.42 (m, 1H), 6.30 (m, 1H), 5.93, 5.92 (2s, 2H), 4.74 (s, 1H), 4.36 (m, 4H), 2.93 (s, 6H), 1.31 (t, J=7.2, 6H).
Workup
- washwashed with water, 2N HCl, water and brine
- dry with materialThe organic phase was dried over sodium sulfate
- concentrationconcentrated in vacuo
- customThe residue was purified by chromatography (3:1 hexane/EtOAc)
Sources & evidence
- ORD record
- ord-c18e14163bca4fb3aaa3287112574a66
- Source dataset
- uspto-grants-2009_03
- Patent number
- US07507762B2
Reaction notes
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