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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368888Generated: November 2, 2026

Ammonium Chloride → HCID 86588566, compound

https://huagongshe.com/reaction/1368888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantPivaloyl chlorideHCID 62493—
Reactant4-Oxohexanoic acidHCID 3799774—
ReactantHCID 86588567HCID 86588567—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 86588566HCID 8658856663.1%

Reaction Steps

4-Oxohexanoic acid (56.2 μl) was dissolved in methylene chloride (1.4 ml), and the solution was added with triethylamine (98.5 μl) and pivalic chloride (58.0 μl) and stirred under an argon atmosphere at room temperature for 15 minutes. The resulting mixture was added to a methylene chloride (1.4 ml) solution of the crude benzyl (S)-2-((1-amino-2-methylpropyl)(benzyloxyphosphinoyl)oxy)-6-benzyloxycarbonylaminohexanate (140.5 mg) obtained in the step (e) of Example 24, and the mixture was further stirred at room temperature for 4 hours. Saturated aqueous ammonium chloride was added to the mixture, and then the organic substances were extracted with ethyl acetate and the organic layer was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (15 g, hexane:acetone=3:1) to obtain benzyl (S)-6-benzyloxycarbonylamino-2-((2-methyl-1-(5-oxohexanoylamino)propyl)(benzyloxyphosphinoyl)oxy)hexanoate (105.4 mg, 63.1%). This compound was subjected to the measurement of molecular weight and then used in the following reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576627B1
Source datasetuspto-grants-2003_06
ORD IDord-84fd4438ced14b6b9bb13c6a5122da47
Source noteuspto-grants-2003_06