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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251366Generated: November 2, 2026

Methyl iodide → HCID 22272437, compound

https://huagongshe.com/reaction/2251366

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 numberUS07319097B2
Source datasetuspto-grants-2008_01
ORD IDord-a3e87e32835c4043aeeed9c46fda67b5
Source noteuspto-grants-2008_01