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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455682Generated: October 30, 2026

Triethylamine → 5-Chloro-N-{2-[1-(cyanomethyl)-4-piperidinyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl}-2-thiophenecarboxamide

https://huagongshe.com/reaction/1455682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromoacetonitrileHCID 11534—
Reactant5-chloro-N-[1,3-dioxo-2-(4-piperidinyl)-2,3-dihydro-1H-isoindol-4-yl]-2-thiophenecarboxamideHCID 12074893—
SolventDimethylformamideHCID 6228—
Product5-Chloro-N-{2-[1-(cyanomethyl)-4-piperidinyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl}-2-thiophenecarboxamideHCID 12073245—

Reaction Steps

A mixture of 100 mg (0.26 mmol) of 5-chloro-N-[1,3-dioxo-2-(4-piperidinyl)-2,3-dihydro-1H-isoindol-4-yl]-2-thiophenecarboxamide, 0.022 ml (0.31 mmol) of α-bromoacetonitrile and 0.072 ml (0.51 mmol) of triethylamine in 2.5 ml of DMF are stirred at room temperature overnight. The mixture is concentrated and the residue is taken up in dichloromethane, washed with sodium bicarbonate solution, dried over magnesium sulfate and concentrated. The product is crystallized with ether, filtered off with suction and dried under high vacuum. Alternatively, the product can be purified by chromatography on silica gel (dichloromethane/methanol mixtures).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482472B2
Source datasetuspto-grants-2009_01
ORD IDord-8ca8be8ec894491a82eb4e2ef49e10c4
Source noteuspto-grants-2009_01