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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645661Generated: October 31, 2026

2-Chloronicotinonitrile → HCID 58996706, compound

https://huagongshe.com/reaction/645661

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloronicotinonitrileHCID 81079—
ReactantPotassium BicarbonateHCID 516893—
ReactantTert-butyl 1,4-diazepane-1-carboxylateHCID 2756058—
SolventDimethylformamideHCID 6228—
ProductHCID 58996706HCID 58996706—

Reaction Conditions

Temperature90 °C

Reaction Steps

2-Chloro-nicotinonitrile (1.0 g, 7.215 mmol) was added to a mixture of [1,4]Diazepane-1-carboxylic acid tert-butyl ester and potassium hydrogencarbonate (0.87 g, 8.66 mmol) in N,N-dimethylformamide (20 mL). The mixture was heated at 90° C. overnight. The reaction mixture was poured onto ice and extracted with dichloromethane. The organic layer was washed with water and brine then dried over magnesium sulfate and filtered. The solvent was removed and the residue was purified by flash column chromatography on silica using ethyl acetate/heptane (50:50) mixture as the mobile phase to give 4-(2-Cyano-phenyl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester. 1H-NMR (400 MHz, DMSO-d6) δ 1.25 (d, 27 Hz, 9H), 1.81 (m, 1H), 1.87 (m, 1H), 3.31 (m, 2H), 3.55 (m, 1H), 3.60 (m, 1H), 3.84 (m, 2H), 3.94 (m, 2H), 6.75 (m, 2H), 8.34 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07704997B1
Source datasetuspto-grants-2010_04
ORD IDord-fc561597d41c4c77aed294a2ea2d504f
Source noteuspto-grants-2010_04