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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743135Generated: November 3, 2026

Ethyl 3-isocyanatobenzoate → Ethyl 3-(2-benzyl-2-azabicyclo[2.2.1]hept-7-ylmethoxycarbonylamino)benzoate

https://huagongshe.com/reaction/1743135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-isocyanatobenzoateHCID 589806—
Reactant(2-Benzyl-2-azabicyclo[2.2.1]hept-7-yl)methanolHCID 9942599—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(2-benzyl-2-azabicyclo[2.2.1]hept-7-ylmethoxycarbonylamino)benzoateHCID 1027286658.6%

Reaction Steps

200.00 mg (0.920 mmol) of (2-benzyl-2-aza-bicyclo[2.2.1]hept-7yl)methanol were dissolved in 3 ml of dry THF and then 176.00 mg (0.920 mmol) of ethyl 3-isocyanatobenzoate in 1 ml of dry THF were added at room temperature. After stirring for 6 hours at room temperature, 125 mg (0.30 mmol) of tris-(2-aminoethyl)amine-polystyrene and 250 mg (0.30 mmol) of methyl isocyanate-polystyrene (each from NovaBiochem) were added and stirred at 50° C. overnight. After the resins had been filtered off, the solvent was removed and the required product was purified by chromatography with ethyl acetate as mobile phase. In this way, 220.00 mg (0.539 mmol) of ethyl 3-(2-benzyl-2-azabicyclo[2.2.1]hept-7-ylmethoxycarbonylamino)benzoate were obtained in the form of a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07008955B2
Source datasetuspto-grants-2006_03
ORD IDord-b62b452f58ed43caaf6d5b27fede0eb1
Source noteuspto-grants-2006_03