Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806285Generated: October 30, 2026

2-Propylpyrrolidine → 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-{5-[(2-propyl-1-pyrrolidinyl)methyl]-3-thienyl}-1H-indole-7-carboxamide

https://huagongshe.com/reaction/1806285

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PropylpyrrolidineHCID 3795961—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(5-formyl-3-thienyl)-1H-indole-7-carboxamideHCID 57732703—
SolventDimethyl SulfoxideHCID 679—
Product3-[1-(ethylsulfonyl)-4-piperidinyl]-5-{5-[(2-propyl-1-pyrrolidinyl)methyl]-3-thienyl}-1H-indole-7-carboxamideHCID 1603782238.7%

Reaction Steps

To a solution of 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(5-formyl-3-thienyl)-1H-indole-7-carboxamide (50 mg, 0.11 mmol) in DMSO (2.0 mL) was added 2-propylpyrrolidine (113 mg, 1.0 mmol). The reaction mixture was then reacted in a microwave at 120° C. for 10 min. Sodium triacetoxyborohydride (220 mg, 1.0 mmol) was then added and the reaction was reacted at room temperature overnight. It was then purified by Gilson Preparatory HPLC to give 21.0 mg of the title compound (38.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354406B2
Source datasetuspto-grants-2013_01
ORD IDord-e43d4961683148dd9aca511be9b88abf
Source noteuspto-grants-2013_01