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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 반응물 | 1-(6,6-Dibromo-7-oxo-4,5,6,7-tetrahydro-2-benzothiazolyl)-3-ethyl-urea | HCID 21985529 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-(6-Bromo-7-hydroxy-2-benzothiazolyl)-3-ethylurea | HCID 21985595 | 78% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07091227B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-4f2e74aefc354a3f8e93f452a584a7ad |
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| 출처 메모 | uspto-grants-2006_08 |
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