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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582587Generated: November 1, 2026

HCID 15407200, compound → HCID 517029, compound

https://huagongshe.com/reaction/1582587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15407200HCID 15407200—
ReactantHCID 178449450HCID 178449450—
SolventDichloromethaneHCID 6344—
ProductHCID 517029HCID 517029—

Reaction Steps

Under an argon atmosphere, a dichloromethane (15 ml) solution of the 2-methyl-1-(3-phenylpropanoylamino)propylphosphinic acid (162 mg) obtained in the above step (a) was added with benzyl (S)-6-benzyloxycarbonylamino-2-hydroxyhexanoate (228 mg) which was obtained from 6-amino-2-hydroxyhexanoic acid described in Chem. Pharm. Bull., 621(1976) in a conventional manner, N-(dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (180 mg), and dimethylaminopyridine (38.7 mg), and then the mixture was stirred at room temperature for 16 hours. The organic substances were extracted with ethyl acetate, and the extract was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by silica gel column chromatography (10 g, chloroform:methanol=10:1) to obtain benzyl (S)-6-(benzyloxycarbonylamino)-2-((2-methyl-1-(3-phenylpropanoylamino)propyl)phosphinoyloxy)hexanoate (117 mg, 31%). This compound was subjected to the measurement of molecular weight and then used in the following reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06737416B2
Source datasetuspto-grants-2004_05
ORD IDord-65ede753e7ba42bd85c480bde2960398
Source noteuspto-grants-2004_05