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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 271786생성일: 2026년 10월 26일

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/271786

반응식

참여 물질

역할이름HCID투입량
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물3-Chloro-1,2-benzoxazoleHCID 2779780—
용매PyridineHCID 1049—
생성물4-Benzo[d]isoxazol-3-yl-piperazine-1-carboxylic acid tert-butyl esterHCID 5925231642%

반응 조건

온도100 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07452890B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-6fd1099501c54868937e6a852b7d364b
출처 메모uspto-grants-2008_11