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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702972Generated: October 30, 2026

HCID 131712164, compound → HCID 131712166, compound

https://huagongshe.com/reaction/1702972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131712164HCID 131712164—
SolventMethanolHCID 887—
ProductHCID 131712166HCID 13171216666%

Reaction Steps

There was added 2 ml of N-sodium hydroxide to a solution of 0.556 g (0.001 mole) of N-carbobenzoxy-L-prolyl-dehydrophenylalanyl-L-phenylalanine methyl ester in 10 ml of methanol. The mixture was stirred at room temperature for 2 hours and concentrated in vacuo. The residual aqueous solution was washed with ethyl acetate and after acidification with 4 N-hydrochloric acid, the resulting separated oil was extracted into ethyl acetate and the extracts were dried over anhydrous Na2SO4. The solvent was evaporated in vacuo and the residual oil was purified on a column of silica gel (60-200 mesh) by elution with ether. The oily product was crystallized from ether to yield 0.357 g (66%) of N-carbobenzoxy-L-prolyl-dehydrophenylalanyl-L-phenylalanine, mp 171°-173°, RfA 0.68, [α]D26 =-30.2° (c, 1% in THF); ir (CHCl3) 1730 (Sh, C=O), 1670 (C=O), 1630 cm-1 (Sh,C=C); NMR (CDCl3) δ1.5-2.3 (m, 4H, Pro ring), 3.0-3.5 (m, 2H, >CH--CH2Ph), 3.2-3.7 (m, 2H, Pro ring), 4.2-4.5 (m, 1H>CHCH2Ph), 4.6-5.0 (m, 1H, Pro ring), 5.0 (s, 2H, >N--OCOCH2Ph), 7.0-7.6 (m, 16H, ArH and PhCH=C--), 8.0-8.27 (br, 1H, --NH exchanged by D2O); 9.03-9.5 (br, 2H, --NH or --COOH, exchanged by D2O.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04350628
Source datasetuspto-grants-1982_09
ORD IDord-acd4e8dc927b46e18a92bccd55c391ea
Source noteuspto-grants-1982_09