Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192775Generated: November 2, 2026

1-Hydroxybenzotriazole → HCID 86649289, compound

https://huagongshe.com/reaction/2192775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-Methylpiperidin-4-ol hydrochlorideHCID 21949295—
Reactant(3R*,5S*)-1-(tert-butoxycarbonyl)-5-[({2-tert-butyl-4-[(2-furylmethyl)amino]pyrimidin-5-yl}carbonyl)(isobutyl)amino]piperidine-3-carboxylic acidHCID 59625458—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
ProductHCID 86649289HCID 8664928994.3%

Reaction Steps

(3R*,5S*)-1-(tert-Butoxycarbonyl)-5-[({2-tert-butyl-4-[(2-furylmethyl)amino]pyrimidin-5-yl}carbonyl)(isobutyl)amino]piperidine-3-carboxylic acid (100 mg), HOBt (41 mg) and WSC.HCl (52 mg) were dissolved in acetonitrile (3 ml), 4-methylpiperidin-4-ol monohydrochloride (27 mg) and triethylamine (75 μl) were added and the mixture was stirred at room temperature for 15 hr. The reaction mixture was concentrated, the residue was diluted with water, 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 and the residue was purified by silica gel column chromatography. The fraction eluted with ethyl acetate-hexane (1:5-3:1) was concentrated under reduced pressure to give the object compound (110 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329691B2
Source datasetuspto-grants-2012_12
ORD IDord-437778e8b1e94f19bccafca079ffdcdb
Source noteuspto-grants-2012_12