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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496283Generated: October 30, 2026

Water → HCID 12071670, compound

https://huagongshe.com/reaction/496283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantPhenyl chloroformateHCID 15891—
Reactant6-(1-PIPERIDINYL)-3-PYRIDINAMINEHCID 10241353—
SolventDichloromethaneHCID 6344—
ProductHCID 12071670HCID 12071670—

Reaction Steps

3,4,5,6-Tetrahydro-2H-[1,2′]bipyridinyl-5′-ylamine (1.01 g, 5.7 mmol) and pyridine (12 ml) are stirred in dry CH2Cl2. Phenylchloroformate (1.3 g, 8.5 mmol) is added to this mixture and stirred for 24 h at room temperature. Water and a solution of 1:1 EtOAc/hexanes is added and the organic layer is separated. The organic layer is washed with 1N HCl three times and with brine once. The organic layer is dried over Na2SO4, filter, and evaporated in vacuo. Purify by flash column chromatography (0-10% EtOAc/CH2Cl2) to obtain (3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-5′-yl)-carbamic acid phenyl ester. Mass spec.: M−1=280 (AP−). B. 1′(6-piperidyl-pyridin-3-yl-carbamoyl)-spiroisobenzofuran-1,4′-piperidine

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06943199B2
Source datasetuspto-grants-2005_09
ORD IDord-95fc91c81192446d8d73296eec631f74
Source noteuspto-grants-2005_09