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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491867Generated: October 26, 2026

1-Hydroxybenzotriazole → [Cyclohexyl-(methoxy-methyl-carbamoyl)-methyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/491867

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant(2R)-[(tert-Butoxycarbonyl)amino](cyclohexyl)acetic acidHCID 7014890—
Reactant1,3-Dimethylaminopropyl-3-ethylcarbodiimideHCID 23063873—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product[Cyclohexyl-(methoxy-methyl-carbamoyl)-methyl]-carbamic acid tert-butyl esterHCID 72442761—

Reaction Steps

To an ice cooled solution of Boc-D-cyclohexylglycine (10 g, 39 mmol) in DCM (200 mL), N,O-dimethylhydroxyamine HCl salt (4.6 g, 46 mmol), HOBT (7 g, 51 mmol), and TEA (11 mL) were added followed by addition of 1,3-dimethylamino propyl-3-ethylcarbodiimide (EDC, 10 g, 51 mmol). The reaction mixture was allowed to warm to room temperature and then stirred overnight. EtOAc (300 mL) was added. The resulting solution washed with aqueous citric acid solution, aqueous NaHCO3 solution, and aqueous NaCl solution. The organic layer was separated, dried with MgSO4, and then evaporated to yield [cyclohexyl-(methoxy-methyl-carbamoyl)-methyl]-carbamic acid tert-butyl ester as a colorless oil, which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531545B2
Source datasetuspto-grants-2009_05
ORD IDord-4a6ecf75d0b94cc69bc799803035ae23
Source noteuspto-grants-2009_05