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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72532Generated: October 30, 2026

(S)-Methyl 4-(1-aminoethyl)benzoate hydrochloride → methyl 4-((1S)-1-(5-chloro-2-(3-(4-fluorophenoxy)pyrrolidin-1-yl)nicotinamido)ethyl)benzoate

https://huagongshe.com/reaction/72532

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-Methyl 4-(1-aminoethyl)benzoate hydrochlorideHCID 57462942—
Reactant5-Chloro-2-(3-(4-fluorophenoxy)pyrrolidin-1-yl)nicotinic acidHCID 67958506—
Productmethyl 4-((1S)-1-(5-chloro-2-(3-(4-fluorophenoxy)pyrrolidin-1-yl)nicotinamido)ethyl)benzoateHCID 6795866840.2%

Reaction Steps

The title compound (D193) (64 mg) was prepared according to the experimental procedure described in Description 146 starting from 5-chloro-2-(3-(4-fluorophenoxy)pyrrolidin-1-yl)nicotinic acid (D138) (110 mg, 0.320 mmol), and (S)-methyl 4-(1-aminoethyl)benzoate (D3) (68.82 mg, 0.320 mmol) MS: (ES/+) m/z: 499.2 [MH+] C26H25ClFN3O4 requires 497.15

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828987B2
Source datasetuspto-grants-2014_09
ORD IDord-dd7684be12774ab6b9f2d3e32af4ef33
Source noteuspto-grants-2014_09