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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262883Generated: October 31, 2026

Diphenylphosphinic chloride → HCID 70510866, compound

https://huagongshe.com/reaction/1262883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenylphosphinic chlorideHCID 73910—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-[(1,1-Dimethylethoxy)carbonyl]-O-(1,1-dimethylethyl)-N-methyl-L-tyrosineHCID 54000823—
ReactantHCID 70510997HCID 70510997—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70510866HCID 70510866—

Reaction Conditions

Temperature-20 °C

Reaction Steps

Diisopropylethylamine (0.90 ml.), then diphenylphosphinyl chloride (1.23 g.), were added to a solution of N-(tert-butyloxycarbonyl)-O-(tert-butyl)-N-methyl-L-tyrosine (1.76 g.) in tetrahydrofuran (15 ml.) maintained at -20° C., and the mixture was stirred for ten minutes. A solution of N-(3-phenylpropyl)-D-methioninamide hydrochloride (1.58 g.) and diisopropylethylamine (0.90 ml.) in tetrahydrofuran (10 ml.) was then added. The mixture was stirred for one half hour at -20°, one hour at 0° C. and overnight at room temperature, then filtered and stripped of solvent. A solution of the residue in ethyl acetate (100 ml.) was washed with water, aqueous citric acid, water again, aqueous sodium bicarbonate and water again, dried and stripped of solvent. Purification of the residue by high pressure liquid chromatography on silica gel (350 g.) using hexane-ethyl acetate (2:1) as the eluant afforded in fractions 6-7 (k'=8-14) [N-(tert-butyloxycarbonyl)-O-(tert-butyl)-N-methyl-L-tyrosyl]-N-(3-phenylpropyl)-D-methioninamide as a clear gum (2.1 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04454120
Source datasetuspto-grants-1984_06
ORD IDord-214dff10a3984679bf10cc884e0c0e85
Source noteuspto-grants-1984_06