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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340742Generated: October 30, 2026

Ammonia → tert-Butyl 6-carbamoyl-3-azabicyclo[3.1.0]hexane-3-carboxylate

https://huagongshe.com/reaction/340742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-((Tert-butoxy)carbonyl)-3-azabicyclo(3.1.0)hexane-6-carboxylic acidHCID 53395288—
ReactantHCID 178418385HCID 178418385—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 6-carbamoyl-3-azabicyclo[3.1.0]hexane-3-carboxylateHCID 7022202770.6%

Reaction Steps

The 3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid (252 mg, 1.11 mmol) prepared in Example 3, benzotriazole (180 mg, 1.33 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (255 mg, 1.33 mmol) were dissolved in 3.0 mL of methylene chloride and diisopropylethylamine (232 μL, 1.33 mmol) was added dropwise. After adding 2 M ammonia solution (2.49 mL, 4.98 mmol) dissolved in methanol dropwise at 0° C., the mixture was stirred at room temperature for 4 hours. The completion of the reaction was confirmed by TLC (CH2Cl2:MeOH=15:1). After the reaction was completed, the reaction mixture was diluted with methylene chloride and washed with saturated sodium chloride. The organic layer was dried with anhydrous magnesium sulfate, filtered, concentrated under reduced pressure and separated by column chromatography (CH2Cl2:MeOH=15:1) to obtain 177 mg (70.6%) of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895602B1
Source datasetuspto-grants-2014_11
ORD IDord-c35230e87fdb4aa1901580654cb8efea
Source noteuspto-grants-2014_11