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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768835Generated: November 1, 2026

2(R)-(4-Methoxybenzyl)-3-(morpholinocarbonyl)propionic acid → (2R, 4S, 5S)-N-Butyl-6-cyclohexyl-4-hydroxy-5-{N-[2(R)-(4-methoxybenzyl)-3-(morpholinocarbonyl)propionyl]-3-(4-thiazolyl)-L-alanyl}amino-2-methylhexanamide

https://huagongshe.com/reaction/1768835

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2(R)-(4-Methoxybenzyl)-3-(morpholinocarbonyl)propionic acidHCID 14429473—
Reactant(2R, 4S, 5S)-5-[N-(t-butoxycarbonyl)-3-(4-thiazolyl)-L-alanyl]amino-N-butyl-6-cyclohexyl-4-hydroxy-2-methylhexanamideHCID 15045764—
Product(2R, 4S, 5S)-N-Butyl-6-cyclohexyl-4-hydroxy-5-{N-[2(R)-(4-methoxybenzyl)-3-(morpholinocarbonyl)propionyl]-3-(4-thiazolyl)-L-alanyl}amino-2-methylhexanamideHCID 1504573559.2%

Reaction Steps

The procedure described in Example 6(b) was repeated, but using 200 mg (0.36 mmole) of (2R, 4S, 5S)-5-[N-(t-butoxycarbonyl)-3-(4-thiazolyl)-L-alanyl]amino-N-butyl-6-cyclohexyl-4-hydroxy-2-methylhexanamide [prepared as described in Example 6(a)] and 110 mg (0.36 mmole) of 2(R)-(4-methoxybenzyl)-3-(morpholinocarbonyl)propionic acid, to afford 158 mg of the title compound as a white powder, melting at 130°-132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05378689
Source datasetuspto-grants-1995_01
ORD IDord-40eaecc72a1d45dc9721706ec5a1fc78
Source noteuspto-grants-1995_01