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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356764Generated: October 30, 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/356764

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 numberUS05837873
Source datasetuspto-grants-1998_11
ORD IDord-a1cf27a880ff42d28daac0eabf5c883a
Source noteuspto-grants-1998_11