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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715223Generated: November 5, 2026

1-(6-(3,3,3-Trifluoropropoxy)pyridin-3-yl)ethanamine hydrochloride → 4-chloro-2-(1-(6-(3,3,3-trifluoropropoxy)pyridin-3-yl)ethyl)-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-1-one

https://huagongshe.com/reaction/715223

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(6-(3,3,3-Trifluoropropoxy)pyridin-3-yl)ethanamine hydrochlorideHCID 67509338—
ReactantMethyl 3-(bromomethyl)-2-chloropyridine-4-carboxylateHCID 72213786—
Product4-chloro-2-(1-(6-(3,3,3-trifluoropropoxy)pyridin-3-yl)ethyl)-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-1-oneHCID 8987503147%

Reaction Steps

The title compound is prepared in 47% yield (102 mg, colorless oil) from methyl 3-(bromomethyl)-2-chloroisonicotinate (150 mg, 0.57 mmol) and 1-(6-(3,3,3-trifluoropropoxy)pyridin-3-yl)ethanamine hydrochloride (154 mg, 0.57 mmol, Amine-15, single enantiomer) in a similar manner to Intermediate-2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187475B2
Source datasetuspto-grants-2015_11
ORD IDord-133c61a8cfef482b927787a9a1638edb
Source noteuspto-grants-2015_11