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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855751Generated: October 29, 2026

Benzyloxycarbonyl-prolyl-histidyl-leucine, tert-Butyl Ester → HCID 178445971, compound

https://huagongshe.com/reaction/1855751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyloxycarbonyl-prolyl-histidyl-leucine, tert-Butyl EsterHCID 178445970—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 178445971HCID 178445971116.4%

Reaction Steps

A mixture of the protected tripeptide of formula III, Z-Pro-His-Leu-OBut (5.9 g, 10.6 mmol, described in Example 2), and 5% palladium on carbon (600 mg) in glacial acetic acid is subjected to hydrogenation. The mixture is filtered and the filtrate evaporated under reduced pressure to give 5.2 g of H-Pro-His-Leu-OBut in the form of its acetate salt. This product is suspended in toluene and the toluene then is removed by distillation so the excess acetic acid is removed azeotropically.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04216209
Source datasetuspto-grants-1980_08
ORD IDord-982213a31ea14dedb9d257f46a607fca
Source noteuspto-grants-1980_08