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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9108생성일: 2026년 10월 25일

1,8-Diazabicyclo(5.4.0)undec-7-ene → 1-(6-Bromo-7-hydroxy-2-benzothiazolyl)-3-ethylurea

https://huagongshe.com/reaction/9108

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참여 물질

역할이름HCID투입량
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물1-(6,6-Dibromo-7-oxo-4,5,6,7-tetrahydro-2-benzothiazolyl)-3-ethyl-ureaHCID 21985529—
용매TetrahydrofuranHCID 8028—
생성물1-(6-Bromo-7-hydroxy-2-benzothiazolyl)-3-ethylureaHCID 2198559578%

반응 조건

온도20 °C

반응 단계

A suspension of 1-(6,6-dibromo-7-oxo-4,5,6,7-tetrahydro-2-benzothiazolyl)-3-ethyl-urea 5 (7.78 g, 19.6 mmol) in THF (50 mL) was treated with DBU (8.79 mL, 58.8 mmol, 3.0 eq) dropwise at about 20° C. A dark green suspension was obtained while heat was generated upon addition of DBU. It was stirred at about 20° C. for about 18 hours. The reaction mixture was concentrated and the residue was treated with saturated NH4Cl (aq) solution to neutral. A light brown colored precipitate was obtained. It was filtered off and washed with H2O (2×50 mL), small amount of MeOH and CH2Cl2, and finally dried under vacuum to give 4.83 g (78%) of the desired compound 6. 1H NMR (DMSO) δ 10.68 (br s, 1H, NH), 7.43 (d, 1H, J=8.5 Hz, ArH), 7.08 (d, 1H, J=8.5 Hz, ArH), 6.70 (br s, 1H, NH), 3.18 (m, 2H, CH2), 1.09 (t, 3H, J=7.2 Hz, CH3). LC/MS 316 (MH+); RP-HPLC RT 2.80 minutes.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091227B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-4f2e74aefc354a3f8e93f452a584a7ad
출처 메모uspto-grants-2006_08