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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970141Generated: October 28, 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/970141

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant3-Chloro-1,2-benzoxazoleHCID 2779780—
SolventPyridineHCID 1049—
Product4-Benzo[d]isoxazol-3-yl-piperazine-1-carboxylic acid tert-butyl esterHCID 5925231642%

Reaction Conditions

Temperature100 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07309703B2
Source datasetuspto-grants-2007_12
ORD IDord-23e37499951545e6bf55cdbc5fb5a311
Source noteuspto-grants-2007_12