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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629949Generated: October 29, 2026

(R)-3-((R)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-tert-butoxy-3-oxopropylthio)propane-1,2-diyl didodecanoate → (5R,9R)-9-(dodecanoyloxy)-1-(9H-fluoren-9-yl)-3,12-dioxo-2,11-dioxa-7-thia-4-azatricosane-5-carboxylic acid

https://huagongshe.com/reaction/629949

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-3-((R)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-tert-butoxy-3-oxopropylthio)propane-1,2-diyl didodecanoateHCID 66613539—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
Solventtert-Butyl methyl etherHCID 15413—
Product(5R,9R)-9-(dodecanoyloxy)-1-(9H-fluoren-9-yl)-3,12-dioxo-2,11-dioxa-7-thia-4-azatricosane-5-carboxylic acidHCID 67414703—

Reaction Steps

A solution of (R)-3-((R)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-tert-butoxy-3-oxopropyl thio)propane-1,2-diyl didodecanoate (11) in 40% TFA in DCM (0.3 M) was stirred at room temperature until complete deprotection of tert-butyl group (2 hr). The reaction mixture was diluted in MTBE, washed three times with 1M citric acid (adjusted to pH3), and once with 1:2 1N HCl/brine. The organic layer was dried over anhydrous Na2SO4 and concentrated en vacuo. The resulting waxy solid was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315530B2
Source datasetuspto-grants-2016_04
ORD IDord-1feb95460a424b27b71190798a2864f9
Source noteuspto-grants-2016_04