Benzylamine → HCID 12041751, compound
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[O:7][C:8]2[C:13]([C:14](=[O:16])[CH:15]=1)=[CH:12][CH:11]=[C:10](OS(C1C=CC(C)=CC=1)(=O)=O)[C:9]=2[N+:28]([O-:30])=[O:29])=[O:5])[CH3:2].[CH2:31]([NH2:38])[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1>ClC1C=CC=CC=1Cl.C(OCC)(=O)C>[CH2:1]([O:3][C:4]([C:6]1[O:7][C:8]2[C:13]([C:14](=[O:16])[CH:15]=1)=[CH:12][CH:11]=[C:10]([NH:38][CH2:31][C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1)[C:9]=2[N+:28]([O-:30])=[O:29])=[O:5])[CH3:2]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 170 °C
Procedure
To a solution of 8-nitro-4-oxo-7-(toluene-4-sulfonyloxy)-4H-chromene-2-carboxylic acid ethyl ester (433 mg, 1 mmol) in o-dichlorobenzene was added benzylamine (214 mg, 2 mmol). The reaction mixture was heated at 170° C. for 1 hour, and the solvent was removed in vacuo to give a residue. The residue was dissolved in ethyl acetate and washed sequentially with aqueous HCl (2N 50 ml), NaOH (2N, 50 mL) and water, dried over anhydrous Na2SO4, and filtered. The solvent was evaporated in vacuo to give a solid residue. Recrystallization of the residue from ethyl acetate-hexane (2:1) provided 246 mg (67%) of the title compound: mp 168° C.; 1H NMR (400 MHz, CDCl3): 1.43 (t, J=7 Hz, 3H), 4.45 (q, J=7.0 Hz, 2H), 4.61 (d, J=5.0 Hz, 2H), 6.90 (d, J=9.2 Hz), 7.09 (s, 1H), 7.42-7.32 (m, 5H), 8.04 (t, J=5 Hz, 1H), 8.10 (d, J=9.2 Hz, 1H); IR: 3350, 2980, 1730, 1660, 1600,1420,1250 cm−1; MS 369 [M+H]+.
Workup
- customthe solvent was removed in vacuo
- customto give a residue
- washwashed sequentially with aqueous HCl (2N 50 ml), NaOH (2N, 50 mL) and water
- dry with materialdried over anhydrous Na2SO4
- filtrationfiltered
- customThe solvent was evaporated in vacuo
- customto give a solid residue
- customRecrystallization of the residue from ethyl acetate-hexane (2:1)
Sources & evidence
- ORD record
- ord-d4e429b4dfa34d6dbf969391cfc21b7f
- Source dataset
- uspto-grants-2003_04
- Patent number
- US06541502B1
Reaction notes
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