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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768839Generated: October 30, 2026

2(R)-benzyl-3-(N-benzyl-N-methylaminocarbonyl)propionic acid → (2S, 4S, 5S)-5-{N-[2(R)-Benzyl-3-(N-benzyl-N-methylaminocarbonyl)propionyl]-3-(4-thiazolyl)-L-alanyl}amino-N-butyl-6-cyclohexyl-4-hydroxy-2-isopropylhexanamide

https://huagongshe.com/reaction/1768839

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2(R)-benzyl-3-(N-benzyl-N-methylaminocarbonyl)propionic acidHCID 15045754—
Reactant(2S, 4S, 5S)-5-[N-(t-Butoxycarbonyl)-3-(4-thiazolyl)-L-alanyl]amino-N-butyl-6-cyclohexyl-4-hydroxy-2-isopropylhexanamideHCID 15045763—
Product(2S, 4S, 5S)-5-{N-[2(R)-Benzyl-3-(N-benzyl-N-methylaminocarbonyl)propionyl]-3-(4-thiazolyl)-L-alanyl}amino-N-butyl-6-cyclohexyl-4-hydroxy-2-isopropylhexanamideHCID 1504574350.3%

Reaction Steps

The procedure described in Example 2(b) was repeated, but using 280 mg (0.48 mmole) of (2S, 4S, 5S)-5-[N-(t-butoxycarbonyl)-3-(4-thiazolyl )-L-alanyl]amino-N-butyl-6-cyclohexyl-4-hydroxy-2-isopropylhexanamide [prepared as described in Example 2(a)] and 150 mg (0.48 mmole) of 2(R)-benzyl-3-(N-benzyl-N-methylaminocarbonyl)propionic acid, to afford 187 mg of the title compound as a white powder, melting at 155°-156° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05378689
Source datasetuspto-grants-1995_01
ORD IDord-dbeedbe0e72948b48dbe5897ba8ffd74
Source noteuspto-grants-1995_01