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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339858Generated: November 1, 2026

Methyl iodide → HCID 178489709, compound

https://huagongshe.com/reaction/339858

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178431655HCID 178431655—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
SolventSodium ThiosulfateHCID 24477—
ProductHCID 178489709HCID 17848970943.5%

Reaction Steps

To a solution of 120 mg of 3-(2-cyclohexylamino-6,6-dimethyl-4,4-dioxo-5,6-dihydro-4H-4lambda6-[1,4,3]oxathiazin-5-yl)phenol in 2 ml of NMP were added, at room temperature, 38 mg of potassium tert-butoxide and 97 mg of methyl iodide, and the reaction mixture was stirred at constant temperature for 2.5 hours. The reaction solution was diluted with 60 ml of water, 5 ml of 5% aqueous sodium thiosulfate solution were added, and the mixture was extracted twice with 30 ml of ethyl acetate. The combined organic phases were dried over MgSO4 and concentrated by rotary evaporation, and the residue was purified in a purification laboratory by means of preparative HPLC. The product-containing fraction was lyophilized. This gave the product (54 mg) with a molecular weight of 366.5 g/mol (C18H26N2O4S); MS (ESI): m/e=367 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895547B2
Source datasetuspto-grants-2014_11
ORD IDord-c2c1c3efd02d4311b518937c59f246ab
Source noteuspto-grants-2014_11