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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554718Generated: October 31, 2026

1-Hydroxybenzotriazole → HCID 66781752, compound

https://huagongshe.com/reaction/554718

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 66781561HCID 66781561—
ReactantHCID 66782507HCID 66782507—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 66781752HCID 66781752—

Reaction Steps

To a solution of 2-Amino-N-benzyl-3-(4-tert-butoxy-phenyl)-N-(2,2-diethoxy-ethyl)-propionamide in CH2Cl2(50 ml) was added a solution of (3R)-3-(3-Benzyl-ureido)-hex-5-enoic acid (1.6 g, 6.1 mmol), EDCl (1.17 g, 7.3 mmol, 1.2 eq), HOBt (0.93 g, 7.3 mmol, 1.2 eq), DIEA (2.13 mL, 12.2 mmol 2.4 eq) in CH2Cl2 (100 mL) stirred for 40 min. The reaction mixture was stirred at room temperature for 14 h, and then diluted with EtOAc, washed with water and brine. The organic layer was dried with Na2SO4 and concentrated in vacuo. The crude compound was used next step without further purification. MS ESI 687 (M+H), 709 (M+Na)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08049008B2
Source datasetuspto-grants-2011_11
ORD IDord-826405b2ac6043cd886b679a30a7c6d1
Source noteuspto-grants-2011_11