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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 132934Erstellt: 25. Oktober 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 4-Benzo[d]isoxazol-3-yl-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/132934

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt3-Chloro-1,2-benzoxazoleHCID 2779780—
LösungsmittelPyridineHCID 1049—
Produkt4-Benzo[d]isoxazol-3-yl-piperazine-1-carboxylic acid tert-butyl esterHCID 5925231642%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a stirred solution of 100 mg (0.65 mmol) of 3-chloro-1,2-benzisoxazole in pyridine (1 mL) was added 145 mg of piperazine-1-carboxylic acid tert-butyl ester (0.78 mmol) and 0.18 mL of DBU (0.78 mmol). The mixture was stirred at 100° C. overnight and then partitioned between EtOAC (50 mL) and water (20 mL) and separated. The aqueous layer was extracted with EtOAC (2×30 mL). The combined organic layers were then washed with water (25 mL), brine, dried over Na2SO4, and the solvent was removed under reduced pressure to give crude product. Purification by column chromatography (silica, 60-100% CH2Cl2/hexanes) gave 82 mg (42%) of the desired product as a light yellow solid. MS (electrospray): exact mass calculated for C16H21N3O3, 303.16; m/z found, 326.1 [M+Na]+. 1H NMR (CDCl3, 400 MHz): 7.68 (dt, J=8.02, 0.98 Hz, 1H), 7.52-7.44 (m, 2H), 7.24 (ddd, J=8.42, 6.46, 1.57 Hz, 1H), 3.66-3.61 (m, 4H), 3.56-3.49 (m, 4H), 1.49 (s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07388011B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-6256d9a19efe4f89821f1fd9baeb3097
Quellennotizuspto-grants-2008_06