Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 131723723 | HCID 131723723 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 131723724 | HCID 131723724 | — |
Reaction Steps
To a solution of carbonic acid 7-tert-butoxycarbonylamino-8,8-diethyl-trans-6-mercapto-5,6,7,8-tetrahydro-naphthalen-2-yl ester tert-butyl ester (28.2 mg, 0.062 mmol) in acetone (2 mL) was added the iodomethane (20 μL, 0.31 mmol) and the potassium carbonate (26 mg, 0.18 mmol), and stirred at reflux for 4 h. The mixture was quenched with H2O, diluted with Et2O (50 mL), washed with H2O, brine, dried over MgSO4. The residu was purified by a flash chromatography (10% AcOEt/Hex) (21.2 mg , 73%). 1H NMR (CDCl3): 7.08 (1H, d, J=8.5 Hz, H5), 7.00-6.95 (2H, m, H6 and H8), 4.56 (1H, d, J=11 Hz, NH), 4.09 (1H, t, J=11.0 Hz, CHNH), 3.25-3.00 (3H, m), 2.15 (3H , broad, SCH3), 1.76 (4H, m, CH2), 1.57 (9H, s, t-butyl), 1.50 (9H, s, t-butyl), 0.73 (6H, m, CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06498196B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-920484da09fd44ab94e43bb41acd4ddc |
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| Source note | uspto-grants-2002_12 |
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