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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744683Generated: October 31, 2026

1-Hydroxybenzotriazole → HCID 69545608, compound

https://huagongshe.com/reaction/1744683

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 22228444HCID 22228444—
ReactantHCID 67232495HCID 67232495—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 69545608HCID 6954560853.7%

Reaction Steps

The product of step D (70 mg) was combined with (3R,4R)-1-(tert-butoxycarbonyl)-3-(4-fluorophenyl)piperidine-4-carboxylic acid (0.1971 mmol; 55 mg), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (57 mg) and 1-hydroxybenzotriazole (40 mg) to which methylene chloride (2.5 mL) was added. The reaction mixture was maintained at ambient temperature for 24 h. The reaction mixture was diluted with methylene chloride (100 mL),washed with a saturated solution of sodium bicarbonate, brine and dried (Na2SO4). The drying agent was removed by filtration and the volatiles were removed in vacuo to furnish the crude N-BOC protected product which was purified on silica gel (eluted with 50:50 to 75:25 ethyl acetate:hexane). The N-BOC protected product was dissolved in ethyl acetate (2 mL) and a saturated solution of hydrogen chloride in ethyl acetate (2 mL) was added. The reaction mixture was maintained at ambient temperature for 90 min. The volatiles were removed in vacuo, the crude product was triturated twice with diethyl ether, and the purified product was dried in vacuo to provide 55 mg of the title compound [MS: m/z 484 (MH+)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015235B2
Source datasetuspto-grants-2006_03
ORD IDord-7793446a70e1437ab23e1164f861208c
Source noteuspto-grants-2006_03