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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158517Generated: November 3, 2026

Citric Acid → [1-(5-Hydroxy-5,6-dihydro-4H-cyclopenta[b]thiophen-4-ylcarbamoyl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1158517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantL-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-HCID 77857—
ReactantHCID 59511560HCID 59511560—
SolventDimethylformamideHCID 6228—
Product[1-(5-Hydroxy-5,6-dihydro-4H-cyclopenta[b]thiophen-4-ylcarbamoyl)-2-phenyl-ethyl]-carbamic acid tert-butyl esterHCID 68677751—

Reaction Steps

To a mixture of the racemic cis-4-amino-5,6-dihydro-4H-cyclopenta[b]thiophen-5-ol (17.5 g, 0.112 mol) in dry DMF (400 mL) was added Boc-L-phenylalanin (30.51 g, 0.115 mol) HOBT (15.6 g, 0.115 mol) and EDAC (22.0 g, 0.115 mol). To the stirred mixture was added TEA (16 mL, 0.115 mol) and the mixture was stirred at room temperature overnight. The mixture was added to 5% citric acid and extracted three times with ethyl acetate. The organic phase was washed with brine and saturated sodium hydrogen carbonate (two times). The organic phase was dried with sodium sulphate and evaporated under reduced pressure. Yield: 43 g=95%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807677B2
Source datasetuspto-grants-2010_10
ORD IDord-767a4b185a114d74ae3d52aa09697312
Source noteuspto-grants-2010_10