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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902648Generated: October 30, 2026

3-Bromo-1-propanol → (2-Chloro-3-trifluoromethyl-benzyl)-(2,2-diphenyl-ethyl)-[3-(6-morpholin-4-yl-pyridin-2-yloxy)-propyl]-amine hydrochloride salt

https://huagongshe.com/reaction/902648

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-1-propanolHCID 12308—
Reactant3-[(2-Chloro-3-trifluoromethyl-benzyl)-diphenylethyl-amino]-propan-1-olHCID 57757117—
Reactant5-(3-Hydroxy-benzyl)-ethoxymethyl-1,2,3,4-tetrazoleHCID 68825468—
ReactantHCID 178516081HCID 178516081—
SolventDiethyl EtherHCID 3283—
Product(2-Chloro-3-trifluoromethyl-benzyl)-(2,2-diphenyl-ethyl)-[3-(6-morpholin-4-yl-pyridin-2-yloxy)-propyl]-amine hydrochloride saltHCID 6925358832%

Reaction Steps

Following the procedure of Example 6(d), except 6-morpholin-4-yl-pyridin-2-ol and N-(2,2-Diphenylethyl)-N-(3-hydroxy-propyl)-N-(2-chloro-3-trifluoromethyl-benzyl)amine were used instead of 5-(3-hydroxy-benzyl)-ethoxymethyl-1,2,3,4-tetrazole and 3-bromo-propanol in step 6(d), the title compound was synthesized as the free base. The tertiaryamine was then dissolved in diethyl ether and acidified with 1.0 M HC/diethyl ether to give 90 mg (32% yield) of the title compound as a white solid. MS (ESI) 610.2 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365085B2
Source datasetuspto-grants-2008_04
ORD IDord-83f2a593dbca4e58881708fed225c2f6
Source noteuspto-grants-2008_04