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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386675Generated: October 30, 2026

Pyridine → HCID 66955715, compound

https://huagongshe.com/reaction/2386675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethyl chloroformateHCID 6586—
ReactantCis tert-Butyl 4-aminocyclohexylcarbamateHCID 2756050—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66955715HCID 66955715112.9%

Reaction Steps

Methyl chloroformate (0.468 mL, 6.06 mmol) was added dropwise, over a period of 20 min, under argon atmosphere, at 0° C., to a mixture of (4-amino-cyclohexyl)-carbamic acid tert-butyl ester (1.0 g, 4.67 mmol) and pyridine (0.479 mL, 6.06 mmol) in THF (6 mL) and the resulting mixture was stirred at RT for 24 h. The reaction mixture was then evaporated under reduced pressure and water (300 mL) was added to the solid residue. The resulting mixture was extracted 3 times with EtOAc (100 mL), the combined organics were washed 3 times with water (100 mL), twice with NaHSO4 (aq 1%, 150 mL) and twice with water (150 mL), dried over Na2SO4, filtered and concentrated under reduced pressure. The remaining white solid was mixed with HCl (2.0 M in MeOH, 200 mL) and the resulting mixture was stirred at RT for 5 h. The reaction mixture was then evaporated under reduced pressure to give 1.1 g of (4-amino-cyclohexyl)-carbamic acid methyl ester hydrochloride salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268840B2
Source datasetuspto-grants-2012_09
ORD IDord-2e543b7f386540208b7aff2f6e2a9741
Source noteuspto-grants-2012_09