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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088219Generated: November 3, 2026

Triethylamine hydrochloride → (1R*,2R*,5S*,6R*)-8-Benzyl-2-{(1R*)-1-[3,5-bis(trifluoromethyl)phenyl]-2-phenylmethoxyethoxy}-1-phenyl-6-(tetrazol-5-yl)-8-azabicyclo[3.2.1]octane

https://huagongshe.com/reaction/2088219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamine hydrochlorideHCID 11130—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
Reactant(1R*,2R*,5S*,6R*)-8-Benzyl-2-{(1R*)-1-[3,5-bis(trifluoromethyl)phenyl]-2-phenylmethoxyethoxy}-6-cyano-1-phenyl-8-azabicyclo[3.2.1]octaneHCID 86586768—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(1R*,2R*,5S*,6R*)-8-Benzyl-2-{(1R*)-1-[3,5-bis(trifluoromethyl)phenyl]-2-phenylmethoxyethoxy}-1-phenyl-6-(tetrazol-5-yl)-8-azabicyclo[3.2.1]octaneHCID 17850618953%

Reaction Steps

(1R*,2R*,5S*,6R*)-8-Benzyl-2-{(1R*)-1-[3,5-bis(trifluoromethyl)phenyl]-2-phenylmethoxyethoxy}-6-cyano-1-phenyl-8-azabicyclo[3.2.1]octane (Example 157; 0.7105 g, 1.07 mmol), sodium azide (0.2087 g, 3.21 mmol) and ammonium chloride (0.172 g, 3.21 mmol) in dimethylformamide (10 ml) were heated at 120° C. for 18 hours. A further 3.0 eq of sodium azide and 3.0 eq of triethylamine hydrochloride were added and the mixture heated for a further 18 hours. The mixture was diluted with ethyl acetate and washed with water. The organics were collected, dried (MgSO4) and concentrated in vacuo. The residue was purified by flash column chromatography, eluting with 5% methanol/dichloromethane to give the title compound (400 mg, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06727249B2
Source datasetuspto-grants-2004_04
ORD IDord-624d0a7cfd25463eaf8f27a916c50649
Source noteuspto-grants-2004_04