Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109820Generated: November 1, 2026

Methanol → Nalpha-Benzyloxycarbonyl-histidyl-D-tryptophyl-alanine

https://huagongshe.com/reaction/1109820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantNalpha-Benzyloxycarbonyl-histidyl-D-tryptophyl-alanine Methyl EsterHCID 178501483—
SolventMethanol--water (1/1)HCID 22242641—
ProductNalpha-Benzyloxycarbonyl-histidyl-D-tryptophyl-alanineHCID 178462140—

Reaction Steps

Under an argon atmosphere, the viscous oil containing tripeptide 20 (ca. 0.253 mol), was hydrolyzed in a solution of MeOH (1500 mL), H20 (500 mL) and NaOH (0.08 g/mL, 11.11 g, 0.278 mol). The reaction was allowed to react at room temperature (ca. 25° C.) while being monitored by HPLC. After two days, HPLC analysis indicated that hydrolysis was complete. The solution was concentrated to a residue in vacuo. Water (500 mL) was then added to the residue. The pH of the resulting solution was ca. 10. This aqueous solution was then extracted with EtOAc (2×500 mL). After this extraction the pH of the aqueous layer was ca. 9. All insoluble material in the aqueous layer was collected by vacuum filtration. The pH of the filtrate was then adjusted to ca. 5 with 2N HCl. This resulted in the precipitation of an oil which was isolated from the aqueous layer by decantation. The oil was taken up in a methanol-water solution and concentrated to a residue in vacuo (109.42 g, 0.200 mol, ca. 79% overall yield from dipeptide 26). This isolated material was consistent with 27 by 1H NMR FDMS=547, M+1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05322931
Source datasetuspto-grants-1994_06
ORD IDord-03d6373184ca4d98a707229aefb6e8f8
Source noteuspto-grants-1994_06