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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400089Generated: November 2, 2026

Diisopropylethylamine → HCID 25054678, compound

https://huagongshe.com/reaction/1400089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(Bromomethyl)-3-(trifluoromethyl)benzeneHCID 123061—
ReactantHCID 59233384HCID 59233384—
SolventHydrochloric AcidHCID 313—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
ProductHCID 25054678HCID 25054678109.6%

Reaction Steps

A mixture of (4-methoxy-6-trifluoromethyl-pyridazin-3-yl)-piperidin-4-yl-amine (D8) (0.10 g, 0.36 mmol), 3-trifluoromethyl-benzyl bromide (0.060 ml, 0.29 mmol) and diisopropylethylamine (0.138 ml, 0.79 mmol) in acetonitrile (2 ml) was stirred at room temperature for 16 h. After this period, the solvent was evaporated in vacuo and the crude product purified by short open column chromatography (silica gel; 3% ammonia in methanol (7M)/dichloromethane). The desired fractions were collected and evaporated in vacuo. The product thus obtained was dissolved in a solution 2M of hydrochloric acid in diethyl ether to yield the corresponding hydrochloride salt E4 (0.138 g, 88%) as a solid. C19H20F6N4O.HCl free base requires 434; Found 435 (MH+). Rt (Method 1): 4.73 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906921B2
Source datasetuspto-grants-2014_12
ORD IDord-7c270af2c9c94b389ea2362407568e99
Source noteuspto-grants-2014_12