Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742912Generated: October 29, 2026

Methanol → (2S 3R,4S 5S)-2,5-Bis-(N-(N-((N-methyl-N-((2-amino-4-thiazolyl)methyl)amino)carbonyl)valinyl)amino)-3,4-dihydroxy-1,6-diphenylhexane

https://huagongshe.com/reaction/742912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantIsopropylamineHCID 6363—
Reactant(2S,3R,4S,5S)-2,5-Bis-(N-(N-((N-methyl-N-((2-((((t-butyl)oxy)carbonyl)amino)-4-thiazolyl)methyl)amino)carbonyl)valinyl)amino)-3,4-dihydroxy-1,6-diphenylhexaneHCID 18655498—
SolventChloroformHCID 6212—
Product(2S 3R,4S 5S)-2,5-Bis-(N-(N-((N-methyl-N-((2-amino-4-thiazolyl)methyl)amino)carbonyl)valinyl)amino)-3,4-dihydroxy-1,6-diphenylhexaneHCID 10259923—

Reaction Steps

Using the procedure of Example 58B but replacing the resultant compound of Example 58A with the resultant compound of Example 93 provided, after silica gel chromatography using first 5% then 10% methanol in chloroform followed by 2% isopropylamine/10% methanol in chloroform, 53 mg (38%) of the desired compound (Rf 0.15, 10% methanol in chloroform) as a white solid, m.p. 130°-134° C. Mass spectrum: (M+1)+ =837.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05554783
Source datasetuspto-grants-1996_09
ORD IDord-0b6fb2458d014e28903b0b1fd3c181e8
Source noteuspto-grants-1996_09