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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237683Generated: October 30, 2026

Methyl iodide → HCID 22272437, compound

https://huagongshe.com/reaction/2237683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22272448HCID 22272448—
SolventAcetoneHCID 180—
ProductHCID 22272437HCID 22272437—
ProductHCID 22272519HCID 22272519—

Reaction Steps

MeI (45 μL, 0.72 mmol) was added to a mixture of N-{4-(4-t-butyloxycarbonyl-1,4-diazepan-1-yl)-2-[(methylsulfonyl)amino]phenyl}benzenesulfonamide (0.189 g, 0.36 mmol) and K2CO3 (0.124, 0.90 mmol) in acetone (25 mL). The mixture was stirred at r.t. for 2 h, filtered and the solvent was removed. Columnchromatography (DCM/MeOH/Heptane 4:1:15) gave 110 mg of N-{4-(4-t-butyloxycarbonyl1,4-diazepan-1-yl)-2-[methyl(methylsulfonyl)amino]-phenyl}benzenesulfonamide and 20 mg of N-{4-(4-t-butyloxycarbonyl 1,4-diazepan-1-yl)-2-[(methylsulfonyl)amino]phenyl}-N-methyl-benzenesulfonamide. Boc-deprotection was carried out by dissolving the compounds in small amount of MeOH and adding HCl/ether. The solvent was removed and the products were recrystrallized from MeOH/ether. N-{4-(1,4-diazepan-1-yl)-2-[methyl(methylsulfonyl)amino]phenyl}benzenesulfonamide hydrochloride M+ 1 439.2 Calcd 439.14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718650B2
Source datasetuspto-grants-2010_05
ORD IDord-77d4aae0603d4542a9281815a2a9e3bc
Source noteuspto-grants-2010_05