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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631733Generated: November 3, 2026

1-Hydroxybenzotriazole → HCID 86670119, compound

https://huagongshe.com/reaction/1631733

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-Phenethylamine, (-)-HCID 75818—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 86670107HCID 86670107—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86670119HCID 86670119—

Reaction Steps

To a 50 mL round-bottom flask were added 4-(5-bromo-2-chloropyrimidin-4-yl)morpholine-3-carboxylic acid (PREPARATION x30, 300 mg, 0.930 mmol), 1-hydroxybenzotriazole (126 mg, 0.930 mmol), and (S)-1-phenylethanamine (118 μl, 0.930 mmol) in 1,4-dioxane (9.3 mL) to give a green solution. 1-Ethyl-(3-dimethylaminopropyl)carbodiimide hydrochloride (178 mg, 0.930 mmol) was added to the solution, which was allowed to react at room temperature for 6 hours. The mixture was subsequently partitioned between aqueous saturated NaHCO3 and ethyl acetate. The aqueous layer was extracted with ethyl acetate and the combined organic layers were dried over MgSO4, filtered, and concentrated to give the title compound, which was used without further purification. ESI-MS m/z [M+H]+ calc'd for C17H18BrClN4O2, 425.03. found 425.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791107B2
Source datasetuspto-grants-2014_07
ORD IDord-99846c8c3aee4e259a5c74b7f642d2a7
Source noteuspto-grants-2014_07