Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630294Generated: October 31, 2026

(S)-4-benzyl 1-tert-butyl 2-(4-(4-fluorophenoxy)phenylcarbamoyl)piperazine-1,4-dicarboxylate → (S)-benzyl 3-(4-(4-fluorophenoxy)phenylcarbamoyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1630294

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-4-benzyl 1-tert-butyl 2-(4-(4-fluorophenoxy)phenylcarbamoyl)piperazine-1,4-dicarboxylateHCID 56954160—
SolventHydrochloric AcidHCID 313—
Product(S)-benzyl 3-(4-(4-fluorophenoxy)phenylcarbamoyl)piperazine-1-carboxylateHCID 5695416187.6%

Reaction Steps

Step (b) A flask was charged with (S)-4-benzyl 1-tert-butyl 2-(4-(4-fluorophenoxy)phenylcarbamoyl)piperazine-1,4-dicarboxylate (1.46 g, 2.75 mmol) and hydrogen chloride (4N in dioxane, 10 mL). The mixture was stirred at ambient temperature for 1 hour and then quenched with saturated sodium bicarbonate (aq., 40 mL). The mixture was extracted with ethyl acetate (30 mL) and the extract was washed with deionized water (10 mL) and then brine (10 mL), dried over anhydrous sodium sulfate, filtered and concentrated to give crude (S)-benzyl 3-(4-(4-fluorophenoxy)phenylcarbamoyl)piperazine-1-carboxylate (1.08 g, 2.41 mmol), which was carried forward without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791102B2
Source datasetuspto-grants-2014_07
ORD IDord-ef7a0ab1240841ddaa359e5387c8188c
Source noteuspto-grants-2014_07