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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491878Generated: October 26, 2026

1-Hydroxybenzotriazole → HCID 178454208, compound

https://huagongshe.com/reaction/491878

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Dimethylaminopropyl-3-ethylcarbodiimideHCID 23063873—
Reactant4-tert-butoxycarbonylamino-4-(S)-tetrahydro-pyran-4-yl-butyric acidHCID 57678337—
ReactantHCID 178525080HCID 178525080—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 178454208HCID 178454208—

Reaction Steps

To an ice cooled solution of cis-4-(2-benzyloxy-ethylamino)-cyclohexanecarboxylic acid benzyl ester (3 g, 8.2 mmol), 4-tert-butoxycarbonylamino-4-(S)-tetrahydro-pyran-4-yl-butyric acid (2.4 g, 8.4 mmol) (prepared as in Example 35) and HOBT (2.4 g, 10.5 mmol) in CH2Cl2 (100 mL) was added TEA (2.3 mL), followed by addition of 1,3-dimethylamino propyl-3-ethylcarbodiimide (EDC, 2.0 g, 10 mmol). The reaction mixture was allowed to warm to room temperature and then was stirred overnight. EtOAc (200 mL) was added and the resulting mixture washed with citric acid solution, NaHCO3 solution, and aq. NaCl solution. The organic layer was dried with MgSO4. The EtOAc was evaporated to yield a colorless oil. The colorless oil (crude product) was purified by column chromatography (1:1 EtOAc/Hexane) to yield 4-{(2-benzyloxy-ethyl)-[4-tert-butoxycarbonylamino-4-(S)-(tetrahydro-pyran-4-yl)-butyryl]-amino}-cis-cyclohexanecarboxylic acid benzyl ester as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531545B2
Source datasetuspto-grants-2009_05
ORD IDord-21e67cbef7ce46e9870e900935cf2509
Source noteuspto-grants-2009_05