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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517785Generated: November 1, 2026

Diisopropylethylamine → HCID 86691898, compound

https://huagongshe.com/reaction/517785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Oxa-8-azabicyclo(3.2.1)octane hydrochlorideHCID 53401129—
Reactant4-[5-(chloromethyl)-1H-tetrazol-1-yl]-2-(trifluoromethyl)benzonitrileHCID 66654576—
SolventHydrochloric AcidHCID 313—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 86691898HCID 8669189860.4%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of 4-[5-(chloromethyl)-1H-tetrazol-1-yl]-2-(trifluoromethyl)benzonitrile (Intermediate 24, 1.70 g, 5.91 mmol) and 3-oxa-8-azabicyclo[3.2.1]octane hydrochloride (Intermediate 27, 0.884 g, 5.91 mmol) in acetonitrile (25 mL) was added di-isopropylethylamine (2.06 mL, 11.8 mmol). The reaction was heated to 85° C. and stirred for 6 hours. The reaction was cooled and the solvent removed under vacuum. The residue was partitioned between DCM (100 mL) and water (50 mL). The aqueous layer was separated and extracted with DCM (50 mL). The DCM layers were combined and the solvent removed. The residue was purified by silica chromatography (Biotage SP4, eluting a gradient of ethyl acetate in iso-hexane) to yield a colourless gum. The product was dissolved in a minimum of DCM before the addition of 1N HCl in diethyl ether (10 mL). The solvent was removed from the resulting suspension. The solid obtained was triturated with diethyl ether (5 mL), the ether decanted and the solid dried under vacuum at 40° C. for 18 hours to yield the title compound as a white solid (1.43 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115132B2
Source datasetuspto-grants-2015_08
ORD IDord-9fc2956737e1450882a35223d6d2b5fc
Source noteuspto-grants-2015_08