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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2773Generated: October 26, 2026

Acetonitrile → 5-Pyridin-3-yl-thiophene-2-sulfonic acid [1-(2-amino-5-cyano-benzyl)-2-oxo-pyrrolidin-3-(S)-yl]-amide

https://huagongshe.com/reaction/2773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant5-Pyridin-3-yl-thiophene-2-sulfonyl chlorideHCID 10658976—
Reactant3-(3-(S)-Amino-2-oxopyrrolidin-1-ylmethyl)benzonitrile hydrochlorideHCID 22870786—
Product5-Pyridin-3-yl-thiophene-2-sulfonic acid [1-(2-amino-5-cyano-benzyl)-2-oxo-pyrrolidin-3-(S)-yl]-amideHCID 53688990—

Reaction Steps

The title compound is prepared in CH3CN instead of CH2Cl2 as described in EXAMPLE 1, Part E using 5-pyridin-3-yl-thiophene-2-sulfonyl choride in place of benzo[b]thiophene-2-sulfonyl chloride and substituting 4-amino-[3-(3-(S)-amino-2-oxo-pyrrolidin-1-ylmethyl)]-benzonitrile dihydrochloride for 3-(3-(S)-amino-2-oxo-pyrrolidin-1-ylmethyl)-benzonitrile hydrochloride. The crude product is obtained by diluting with ethyl acetate and washing with saturated sodium bicarbonate (aq), water and brine. The organic layer is dried over MgSO4, filtered and concentrated. The crude product is purified by column chromatography eluting with 50% EtOAc/CH2Cl2 to give a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05731315
Source datasetuspto-grants-1998_03
ORD IDord-657035b18b544c1293249703fa8250ea
Source noteuspto-grants-1998_03