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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768843Generated: November 2, 2026

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

https://huagongshe.com/reaction/1768843

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2(R)-benzyl-3-(N-benzyl-N-methylaminocarbonyl)propionic acidHCID 15045754—
Reactant(2R, 4S, 5S)-5-[N-(t-butoxycarbonyl)-3-(4-thiazolyl)-L-alanyl]amino-6-cyclohexyl-N-ethyl-4-hydroxy-2-methylhexanamideHCID 15045769—
Product(2R, 4S, 5S)-5-{N-[2(R)-Benzyl-3-(N-benzyl-N-methylaminocarbonyl)propionyl]-3-(4-thiazolyl)-L-alanyl}amino-6-cyclohexyl-N-ethyl-4-hydroxy-2-methylhexanamideHCID 1504574629%

Reaction Steps

The procedure described in Example 6(b) was repeated, but using 325 mg (0.62 mmole) of (2R, 4S, 5S)-5-[N-(t-butoxycarbonyl)-3-(4-thiazolyl)-L-alanyl]amino-6-cyclohexyl-N-ethyl-4-hydroxy-2-methylhexanamide [prepared as described in Example 19(a)] and 200 mg (0.64 mmole) of 2(R)-benzyl-3-(N-benzyl-N-methylaminocarbonyl)propionic acid, to afford 129 mg of the title compound as white crystals, melting at 148°-150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05378689
Source datasetuspto-grants-1995_01
ORD IDord-6df18e238ae6445684d6a915b41d3dda
Source noteuspto-grants-1995_01