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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117044Generated: October 31, 2026

Diisopropylethylamine → HCID 59814692, compound

https://huagongshe.com/reaction/2117044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Chloroethyl chloroformateHCID 521305—
ReactantHCID 59814732HCID 59814732—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 59814692HCID 59814692—

Reaction Steps

To a solution of 3-bromo-10-(8-methyl-8-aza-bicyclo[3.2.1]oct-3-yl)-10H-phenothiazine, 3i (1.0 g, 2.49 mmol) in 1,2-dichloroethane (15 mL) were added 1-chloroethyl chloroformate (807 μL, 7.5 mmol) and N,N-diisopropyl-N-ethylamine (1.4 mL, 7.97 mmol). The mixture was heated to reflux for 2.5 h, allowed to cool to rt, and evaporated. The mixture was evaporated and the residue was dissolved dissolved in methanol (15 mL) and heated to reflux for 1 h. After work-up, the residue was purified via flash column chromatography (eluent gradient: 0 to 30% MeOH in EtOAc containing 1% triethylamine) to yield 150 mg of recovered starting material 3i and 382 mg (66%) of title compound 3-bromo-10-piperidin-4-yl-10H-phenothiazine, 4i as a mixture of endo and exo isomers. MS m/z (MH+) 387.1/389.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439239B2
Source datasetuspto-grants-2008_10
ORD IDord-a2fe821948e94590abc0a515990fb927
Source noteuspto-grants-2008_10