Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385281Generated: October 30, 2026

Methyl iodide → HCID 9948559, compound

https://huagongshe.com/reaction/1385281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTriethylamineHCID 8471—
ReactantHCID 178503630HCID 178503630—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 9948559HCID 994855914.3%

Reaction Steps

To solution of 6,6-dimethyl-3-methylthio-1-(tetrazol-5-yl)-4,5,6,7-tetrahydrobenzo[c]thiophen-4-one (62 mg, 0.21 mmol) in DMF (5 mL) containing triethylamine (58 μL, 0.42 mmol) was added iodomethane (13 μL, 0.21 mmol). After stirring for 1 h more iodomethane (39 μL, 0.63 mmol) was added and stirring continued overnight. Ethyl acetate (20 ml) and water (20 mL) were added and the organic layer separated, dried (Na2SO4) and evaporated. The residue was triturated with CH2Cl2:EtOAc (1:1) and the undissolved solid (26 mg; 0.08 mmol) collected by filtration and washed with EtOAc. The filtrate was chromatographed on silica gel, eluting with petrol:EtOAc (2:) to give the title compound (10 mg, 0.03 mmol) as a tan solid. Total mass=36 mg (56%), mp 233-235° C. Found C, 50.26; H, 5.23; N, 17.94%. C13H16N4S2O requires: C,50.63; H, 5.23; N, 18.17%. 1HNMR (250 MHz, CDCl3) δ 1.10 (6H, s), 2.45 (2H, s), 2.65 (3H, s), 3.11 (2H, s), 4.40 (3H, s). MS (ES+) 309 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262103B1
Source datasetuspto-grants-2001_07
ORD IDord-2ef396b0b47849c0bfb82dd152e9f459
Source noteuspto-grants-2001_07