Pyridine → HCID 69001486, compound

HRID 1786527Notes

Reaction equation

HRID 1786527 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

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

  1. washwashed with water, 2N HCl, water and brine
  2. dry with materialThe organic phase was dried over sodium sulfate
  3. concentrationconcentrated in vacuo
  4. 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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