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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367511Generated: October 30, 2026

Dimethylformamide → HCID 66918650, compound

https://huagongshe.com/reaction/1367511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3,3-Difluoroazetidine hydrochlorideHCID 2758247—
ReactantHCID 49835673HCID 49835673—
ReactantHCID 178418300HCID 178418300—
ProductHCID 66918650HCID 6691865057%

Reaction Steps

To a mixture of (1R,2R,4R)-4-Benzenesulfonyl-2-(morpholine-4-carbonyl)-cyclopentanecarboxylic acid cyanomethyl-amide (3 g, 15 mmol, example 1, step 1) in dimethylformamide (40 mL) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (5.86 g, 30 mmol), hydroxybenzotriazole (3.1 g mg, 22 mmol) and ethyldiisopropylamine (15.4 mL, 90 mmol). After 45 mM, 3,3-difluoroazetidine hydrochloride (1.94 g, 15 mmol) was added and the reaction mixture was stirred for 24 h then partitioned between ethyl acetate and an aqueous saturated solution of sodium hydrogenocarbonate. The aqueous layer was extracted with ethyl acetate and the combined organic layers were washed with water then dried over sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography on silica gel with a gradient of cyclohexane/ethyl acetate (2:1 then 1:1 v/v) as eluant to afford the title compound (2.35 g, 57%) as yellow solid. MS (EI): 276.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893099B2
Source datasetuspto-grants-2011_02
ORD IDord-f810af8d968b4aef86433c3d42827e4a
Source noteuspto-grants-2011_02