Sodium Iodide → HCID 10268050, compound
Reaction equation
C([O:5][C:6](=[O:29])[CH2:7][NH:8][C:9]([C:11]1[C:12]2[N:13]=[C:14]([O:27]C)[C:15]([O:25]C)=[N:16][C:17]=2[CH:18]=[C:19]([N+:22]([O-:24])=[O:23])[C:20]=1[CH3:21])=[O:10])(C)(C)C.[I-].[Na+].Cl[Si](C)(C)C>C(#N)C>[CH3:21][C:20]1[C:19]([N+:22]([O-:24])=[O:23])=[CH:18][C:17]2[NH:16][C:15](=[O:25])[C:14](=[O:27])[NH:13][C:12]=2[C:11]=1[C:9]([NH:8][CH2:7][C:6]([OH:29])=[O:5])=[O:10]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred mixture of [(2,3-Dimethoxy-6-methyl-7-nitro-quinoxaline-5-carbonyl)-amino] acetic acid tert-butyl ester (14a) 150 mg (0.37 mmol) and sodium iodide 555 mg (3.7 mmol) in 25 mL acetonitrile is added dropwise chlorotrimethylsilane 0.46 mL (3.7 mmol). After addition was complete, the reaction mixture was refluxed under an atmosphere of nitrogen for 72 hours. The reaction mixture was quenched by pouring into 100 mL water, and the aqueous mixture was concentrated to 10 mL. The residue was mixed with ethyl acetate, and after stirring for 30 minutes, the product precipitated, 35 mg (29%), mp 250° C. (dec.); 1H NMR (DMSO-d6): δ 12.55 (br s, 1H), 8.40 (t, 1H, J=6.3 Hz), 7.84 (s, 1H), 4.07 (d, 2H, J=6.3 Hz), 2.43 (s, 3H); MS (APCI): m/z 323 (M+H). Anal. Calcd. for C12H10N4O7: C, 44.73; H, 3.13; N, 17.39. Found: C, 41.38; H, 3.12; N, 15.79.
Workup
- additionAfter addition
- temperaturethe reaction mixture was refluxed under an atmosphere of nitrogen for 72 hours
- customThe reaction mixture was quenched
- additionby pouring into 100 mL water
- concentrationthe aqueous mixture was concentrated to 10 mL
- additionThe residue was mixed with ethyl acetate
- customthe product precipitated
Sources & evidence
- ORD record
- ord-05e20ae5ce634cf29034865dbc4b81a4
- Source dataset
- uspto-grants-2002_09
- Patent number
- US06455698B1
Reaction notes
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