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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992411Generated: November 2, 2026

1-Hydroxybenzotriazole → HCID 131723571, compound

https://huagongshe.com/reaction/992411

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN-((1,1-dimethylethoxy)carbonyl)-2-methyl-alanineHCID 2733845—
ReactantHCID 131723569HCID 131723569—
SolventDichloromethaneHCID 6344—
ProductHCID 131723571HCID 131723571—

Reaction Steps

In a 50 ml round bottom flask, 0.33 mmol of Boc-Aib was dissolved in 20 ml dry CH2Cl2 and then 0.31 mmol of 1-hydroxybenzotriazole was added while stirring under N2 atmosphere in an ice-bath. 0.35 mmol of 1-ethyl-3-(3′-dimethylaminopropyl)carbodiimide HCL was added in 10 ml dry CH2Cl2 at a fast drop rate and the reaction mixture was stirred for 1 hour at 0° C. 0.30 mmol of (2) in 15 ml of CH2Cl2 was added dropwise and stirring was continued for an additional 18 h at ambient temperature. The reaction mixture was washed with 20 ml of 20% citric acid aqueous solution, 20 ml of saturated NaHCO3 aqueous solution and 20 ml of saturated sodium chloride aqueous solution. The organic layer was separated and dried over anhydrous magnesium sulfate, filtered and concentrated in vacuum. Further purification was done by flash column chromatography (CHCl3/MeOH, 95:5) to afford white solid of Boc-Aib-DTrp-DPro-3-piperidinamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06468974B1
Source datasetuspto-grants-2002_10
ORD IDord-808c74eb5140432184d4658abb3a0eb2
Source noteuspto-grants-2002_10