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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778032Generated: November 1, 2026

Pyridine → Phenyl(5-cyano-4-(thiophen-2-ylmethoxy)pyridin-2-yl)carbamate

https://huagongshe.com/reaction/1778032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenyl chloroformateHCID 15891—
Reactant6-Amino-4-(thiophen-2-ylmethoxy)nicotinonitrileHCID 118036829—
SolventTetrahydrofuranHCID 8028—
ProductPhenyl(5-cyano-4-(thiophen-2-ylmethoxy)pyridin-2-yl)carbamateHCID 131734798—

Reaction Steps

Phenyl chloroformate (3.46 ml, 27.6 mmol) was added drop wise to a mixture of 6-amino-4-(thiophen-2-ylmethoxy)nicotinonitrile (intermediate 284, 2.90 g, 12.54 mmol) and pyridine (4.46 ml, 55.2 mmol) in THF (100 ml) at room temperature. The reaction mixture was stirred for 16 h at room temperature and then partitioned between EtOAc and saturated aqueous NaHCO3 solution, the organic layer washed with saturated brine, dried over MgSO4 and evaporated. The residue was purified by normal phase chromatography: 80 g RediSep® column, eluting with a gradient from heptane to EtOAc. Product containing fractions were combined and evaporated to give the title compound as a beige solid. (UPLC-MS 3) tR 1.14; ESI-MS 352.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266883B2
Source datasetuspto-grants-2016_02
ORD IDord-e2b801949cbb4fe0a5de08cee1f57b77
Source noteuspto-grants-2016_02