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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777965Generated: October 30, 2026

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

https://huagongshe.com/reaction/1777965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenyl chloroformateHCID 15891—
Reactant6-Amino-4-(2-methoxyethoxy)nicotinonitrileHCID 118036841—
SolventTetrahydrofuranHCID 8028—
ProductPhenyl (5-cyano-4-(2-methoxyethoxy)pyridin-2-yl)carbamateHCID 125470569—

Reaction Steps

Phenyl chloroformate (4.93 ml, 39.3 mmol) was added drop wise to a mixture of 6-amino-4-(2-methoxyethoxy)nicotinonitrile (intermediate 20, 3.45 g, 17.86 mmol) and pyridine (6.35 ml, 79 mmol) in THF (100 ml) at room temperature. The reaction mixture was stirred for 5 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 triturated with EtOAc and the product obtained by filtration as a white solid. (UPLC-MS 7) tR 0.97; ESI-MS 314.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266883B2
Source datasetuspto-grants-2016_02
ORD IDord-00483b89a7344602a1df823fcdb0219c
Source noteuspto-grants-2016_02