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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914505Generated: October 26, 2026

Water → 2-{[4-(2-{[(9H-fluorene-9-ylmethoxy)carbonyl]amino}ethyl)-1,3-thiazol-2-yl]thio}-2-methylpropionic acid

https://huagongshe.com/reaction/914505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-{[4-(2-{[(9H-fluorene-9-ylmethoxy)carbonyl]amino}ethyl)-1,3-thiazol-2-yl]thio}-2-methylpropionic acid tert-butyl esterHCID 59759401—
SolventDichloromethaneHCID 6344—
Product2-{[4-(2-{[(9H-fluorene-9-ylmethoxy)carbonyl]amino}ethyl)-1,3-thiazol-2-yl]thio}-2-methylpropionic acidHCID 59759051128.9%

Reaction Steps

To a solution of 2-{[4-(2-{[(9H-fluorene-9-ylmethoxy)carbonyl]amino}ethyl)-1,3-thiazol-2-yl]thio}-2-methylpropionic acid tert-butyl ester (33 g) synthesized in Example 483-1 in dichloromethane (30 mL) was added trifluoroacetic acid (50 mL), and the mixture was stirred at room temperature overnight. The reaction mixture was poured into water, extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over sodium sulfate. The solvent was concentrated under reduced pressure, and purified by silica gel chromatography (elution solvent; ethyl acetate) to give the title compound (38 g) as a pale-brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026370B2
Source datasetuspto-grants-2011_09
ORD IDord-5d1b7865f9f9418383fef6969848d2af
Source noteuspto-grants-2011_09