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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806516Generated: November 1, 2026

Prolinamide, D- → 5-(5-{[(2R)-2-(aminocarbonyl)-1-pyrrolidinyl]methyl}-3-thienyl)-3-[1-[(1-methylethyl)sulfonyl]-4-piperidinyl]-1H-indole-7-carboxamide

https://huagongshe.com/reaction/1806516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantProlinamide, D-HCID 447554—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant5-(5-formyl-3-thienyl)-3-{1-[(1-methylethyl)sulfonyl]-4-piperidinyl}-1H-indole-7-carboxamideHCID 57732783—
CatalystAcetic AcidHCID 176—
SolventDimethyl SulfoxideHCID 679—
Product5-(5-{[(2R)-2-(aminocarbonyl)-1-pyrrolidinyl]methyl}-3-thienyl)-3-[1-[(1-methylethyl)sulfonyl]-4-piperidinyl]-1H-indole-7-carboxamideHCID 5773281867.7%

Reaction Steps

To a solution of 5-(5-formyl-3-thienyl)-3-{1-[(1-methylethyl)sulfonyl]-4-piperidinyl}-1H-indole-7-carboxamide (25 mg, 0.054 mmol) in DMSO (2 mL) was added D-prolinamide (114 mg, 1 mmol) and 2 drops of acetic acid. The resulting mixture was stirred at room temperature for 4 h followed by an addition of sodium triacetoxyborohydride (212 mg, 1.0 mmol). The mixture was reacted overnight. It was then purified by Gilson Preparatory HPLC to give 20.4 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354406B2
Source datasetuspto-grants-2013_01
ORD IDord-b940e0b9117a407998962e6e3f6b9aba
Source noteuspto-grants-2013_01