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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300964Generated: October 30, 2026

Methyl iodide → HCID 131723724, compound

https://huagongshe.com/reaction/2300964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 131723723HCID 131723723—
SolventAcetoneHCID 180—
ProductHCID 131723724HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498196B1
Source datasetuspto-grants-2002_12
ORD IDord-920484da09fd44ab94e43bb41acd4ddc
Source noteuspto-grants-2002_12