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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83635Generated: October 30, 2026

1-Hydroxybenzotriazole → HCID 66571400, compound

https://huagongshe.com/reaction/83635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxylic acidHCID 57385796—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 66571400HCID 66571400—

Reaction Steps

1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxylic acid (100 mg, 0.252 mmol), N1-((ethylimino)methylene)-N3,N3-dimethylpropane-1,3-diamine hydrochloride (72.5 mg, 0.378 mmol), and 1H-benzo[d][1,2,3]triazol-1-ol (51.1 mg, 0.378 mmol) were dissolved in 2.0 mL of DCM and stirred for 10 minutes before the addition of a 2-(4-isopropylphenyl)ethanamine, HCl (75 mg, 0.378 mmol) and N-ethyl-N-isopropylpropan-2-amine (0.132 mL, 0.756 mmol) as a 1.0 mL DCM solution. The reaction was allowed to stir overnight. The reaction was diluted with water and ethyl acetate. The organic layer was washed with 1N HCl, saturated sodium bicarbonate solution, and finally saturated sodium chloride solution. The organic layer was dried over magnesium sulfate, filtered and concentrated. The crude material purified using silica gel chromatography 0-60% ethyl acetate/hexanes. (Yield: 50 mg, white solid) 1H-NMR (500 MHz, DMSO-d6) 7.88, 7.62, 7.55, 7.34, 7.22, 7.18-7.06, 6.71, 5.49, 4.40, 3.97, 3.24, 3.13-2.73, 2.66, 2.40-2.29, 1.79-1.23, 1.16

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846684B2
Source datasetuspto-grants-2014_09
ORD IDord-ad0ab93bdd7047648f60dce817b11468
Source noteuspto-grants-2014_09