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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614873Generated: October 30, 2026

(R)-1-(4-Fluoro-3-methoxyphenyl)ethanamine hydrochloride → (1r/s,3r)-n-[(1r)-1-(4-Fluoro-3-methoxy-phenyl)ethyl]-3-[4-(2-morpholinosulfonylethyl)phenyl]cyclopentanamine

https://huagongshe.com/reaction/1614873

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-1-(4-Fluoro-3-methoxyphenyl)ethanamine hydrochlorideHCID 53484667—
Reactant(3R)-3-{4-[2-(Morpholine-4-sulfonyl)-ethyl]-phenyl}-cyclopentanoneHCID 68751067—
Product(1r/s,3r)-n-[(1r)-1-(4-Fluoro-3-methoxy-phenyl)ethyl]-3-[4-(2-morpholinosulfonylethyl)phenyl]cyclopentanamineHCID 68093342—

Reaction Steps

General procedure B was followed using (3R)-3-{4-[2-(morpholine-4-sulfonyl)-ethyl]-phenyl}-cyclopentanone (preparation 49) as the ketone and (1R)-1-(4-fluoro-3-methoxyphenyl)ethylamine hydrochloride as the amine. 1H NMR (300 MHz, DMSO) δ 7.23-7.04 (m, 6H), 6.92-6.83 (m, 1H), 3.82 (s, 3H), 3.80-3.68 (m, 1H), 3.66-3.55 (m, 4H), 3.37-3.26 (m, 2H), 3.22-3.10 (m, 4H), 3.06-2.78 (m, 4H), 2.20-1.13 (m, 6H), 1.23 (d, J=6.6 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765676B2
Source datasetuspto-grants-2014_07
ORD IDord-5cd45f48cfac47fa94cd6140036aae6e
Source noteuspto-grants-2014_07