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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735865Generated: October 31, 2026

Triethylamine → HCID 19079064, compound

https://huagongshe.com/reaction/1735865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 19079051HCID 19079051—
SolventDichloromethaneHCID 6344—
ProductHCID 19079064HCID 1907906448.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

The following compound was obtained according to a similar manner: ##STR52## MS (FAB) m/e 296 (M+1 for free base) ##STR53## For Compound IN: Dissolved N-[2-(5-ethoxy-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)ethyl]-N-methylamine (150 mg, 0.508 mmol)in 5 mL of dry dichloromethane. Cooled to 0° C. under a nitrogen atmosphere, and added triethylamine (0.14 mL, 0.10 g, 1.0 mmol) and then methanesulfonyl chloride (0.06 mL, 0.089 g, 0.76 mmol) dropwise via syringe. Stirred at 0° C. for 90 mins. Added water, and extracted with dichloromethane. Washed the combined organic extracts with sodium phosphate monobasic, 1N NaOH, and then saturated NaCl. Dried with MgSO4, filtered, and evaporated. Purified crude product by flash chromatography eluting with 9:1 hexane:ethyl acetate. Combined appropriate fractions, and evaporated to solid. Recrystallized from ethyl acetate-hexane to give 92 mg (48% yield) of N-[2-(5-ethoxy-10,11-dihydro-5H-dibenzo[a,d]cycloheptenyl)ethyl]-N-methylmethanesulfonamide as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05538986
Source datasetuspto-grants-1996_07
ORD IDord-3fbab44286eb4152b036a2a608b20944
Source noteuspto-grants-1996_07