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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663431Generated: October 30, 2026

Water → HCID 11709986, compound

https://huagongshe.com/reaction/1663431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 67435312HCID 67435312—
SolventDichloromethaneHCID 6344—
ProductHCID 11709986HCID 1170998648.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

(11S)-11-(Aminomethyl)-10,11-dihydro-8H-[1,4]oxazino[4′,3′:1,2]imidazo[4,5-c]quinolin-6-amine (778 mg, 2.89 mmol) was dissolved in 60 mL of CH2Cl2 and treated with triethylamine (804 μL, 5.78 mmol). The solution was cooled to 0° C. under N2. Methanesulfonyl chloride (224 μL, 2.89 mmol) was then added dropwise. After 75 minutes, the reaction was treated with H2O and extracted repeatedly with 10% methanol/CHCl3. The combined organic layers were washed successively with H2O and brine. The organic portion was dried over Na2SO4, filtered and concentrated under reduced pressure. Chromatography (SiO2, 10-15% methanol/CHCl3) gave an off-white solid. Crystallization from methanol gave N-{[(11S)-6-amino-10,11-dihydro-8H-[1,4]oxazino[4′,3′:1,2]imidazo[4,5-c]quinolin-11-yl]methyl}methanesulfonamide (487 mg) as white, powdery crystals, mp 285-288° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034938B2
Source datasetuspto-grants-2011_10
ORD IDord-a44fb17121f7492e99949ae110b9e2ce
Source noteuspto-grants-2011_10