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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424196Generated: November 1, 2026

Ammonia → HCID 178458084, compound

https://huagongshe.com/reaction/1424196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178460520HCID 178460520—
SolventPyridineHCID 1049—
Solvent1,4-DioxaneHCID 31275—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
ProductHCID 178458084HCID 178458084—

Reaction Steps

A mixture of (3S)-3-[(tert-butoxycarbonyl)amino]-3-(5-tert-butyl-1H-benzimidazol-2-yl)-2-methylpropanoic acid (Preparation 30, 7.25 g, 19.33 mmol), Boc2O (5.9 g, 27.0 mmol), pyridine (1 mL) and NaHCO3 (2 g, 25 mmol) in THF/DMF (200 mL/100 mL) was stirred at room temperature for 18 hours. 0.5M Ammonia in dioxane (150 mL) was added and the reaction continued stirring at room temperature for a further 18 hours. The reaction was concentrated to dryness and diluted with saturated aqueous NaHCO3 solution. The solution was extracted with 2-MethylTHF and concentrated in vacuo. The residue was purified using reverse phase column chromatography eluting with 5-70% acetonitrile in 0.1% formic acid in water to afford the title compound as a mixture of diastereomers (3 g, 43%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927587B2
Source datasetuspto-grants-2015_01
ORD IDord-00a03b1021054958b6a86a5a69b9e8ed
Source noteuspto-grants-2015_01