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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509613Generated: October 28, 2026

Water → HCID 58355136, compound

https://huagongshe.com/reaction/1509613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantHCID 58355160HCID 58355160—
ReactantHCID 178434708HCID 178434708—
SolventTolueneHCID 1140—
ProductHCID 58355136HCID 5835513647.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

(3R,5S)-1-(tert-Butoxycarbonyl)-5-[{[5-(4-methoxybutyl)-1-phenyl-1H-1,2,3-triazol-4-yl]carbonyl}(2-methylpropyl)amino]piperidine-3-carboxylic acid (200 mg) was dissolved in toluene (5 ml), 5-methyl-1H-tetrazole (36 mg) and N,N′-dicyclohexylcarbodiimide (96 mg) were added and the mixture was stirred at 80° C. for 15 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography, and a fraction eluted with ethyl acetate-hexane (1:3-1:1) was concentrated under reduced pressure. The residue was dissolved in toluene (1 ml), trifluoroacetic acid (1 ml) was added and the mixture was stirred at room temperature for 1 hr. The reaction mixture was concentrated under reduced pressure, basified with saturated aqueous sodium hydrogen carbonate, and the mixture was extracted twice with ethyl acetate. The extract was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure. The residue was dissolved in methanol (1 ml), fumaric acid (12 mg) was added and the mixture was concentrated under reduced pressure to give the object product (85 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221836B2
Source datasetuspto-grants-2015_12
ORD IDord-f28525db7e11471b81a0e7ebd470d0c6
Source noteuspto-grants-2015_12