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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230505Generated: November 1, 2026

Methyl iodide → HCID 22272437, compound

https://huagongshe.com/reaction/230505

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. Purification by column chromatography (DCM/MeOH/Heptane 4:1:15) gave 110 mg of N-{4-(4-t-butyloxycarbonyl 1,4-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-[(methylsulfonyl)amino]-phenyl}-N-methylbenzenesulfonamide hydrochloride M+1 439.2 Calcd 439.14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566715B2
Source datasetuspto-grants-2009_07
ORD IDord-4325b8d341ed421b9c525e23421b4ee6
Source noteuspto-grants-2009_07