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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 184Generated: October 26, 2026

5-Chloro-2-nitroanisole → Tert-butyl 4-(3-methoxy-4-nitrophenyl)-3-oxopiperazine-1-carboxylate

https://huagongshe.com/reaction/184

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-nitroanisoleHCID 81110—
ReactantTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
ReagentCesium carbonateHCID 10796—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl 4-(3-methoxy-4-nitrophenyl)-3-oxopiperazine-1-carboxylateHCID 68591567100.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of tert-butyl 3-oxopiperazine-1-carboxylate (1500 mg, 7.49 mmol), 4-chloro-2-methoxy-1-nitrobenzene (1405 mg, 7.49 mmol),cesium carbonate (3417 mg, 10.49 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (195 mg, 0.34 mmol) and TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM (174 mg, 0.19 mmol)was dried for 15 min under HV. Degassed dioxane (17 ml) was added and the resulting mixture was stirred at 90°C for 16 hours under inert atmosphere. Work-up and purification: see EN02378-07-02. tert-butyl 4-(3-methoxy-4-nitrophenyl)-3-oxopiperazine-1-carboxylate (2640 mg, 100 %) was isolated as an orange foam. FLA 02378-10-01: 1H NMR, LC-MS: OK.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-ba7ec5906e7d4fb89a5c2ef7e7a905ac
Source note750 AstraZeneca ELN dataset