Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1042341생성일: 2026년 10월 26일
1,5-Diazabicyclo(4.3.0)non-5-ene → N-[(2-bromo-1,3-thiazol-4-yl)methoxy]-1-(1-methyl-1H-tetrazol-5-yl)-1-phenylmethanimine
https://huagongshe.com/reaction/1042341
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1,5-Diazabicyclo(4.3.0)non-5-ene | HCID 76349 | — |
| 반응물 | 2-Bromo-4-(1-bromoethyl)-1,3-thiazole | HCID 66860748 | — |
| 반응물 | N-hydroxy-1-(1-methyl-1H-tetrazol-5-yl)-1-phenylmethanimine | HCID 135990939 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | N-[(2-bromo-1,3-thiazol-4-yl)methoxy]-1-(1-methyl-1H-tetrazol-5-yl)-1-phenylmethanimine | HCID 86649974 | 568.6% |
반응 단계
To a cooled (0° C.) stirred solution of N-hydroxy-1-(1-methyl-1H-tetrazol-5-yl)-1-phenylmethanimine (0.7 g, 3.44 mmol, 1.0 eq.) in 25 ml of MeCN, was added dropwise DBN (0.42 g, 3.44 mmol, 1.0 eq.). The reaction was stirred for 5 mins before addition of 2-bromo-4-(1-bromoethyl)-1,3-thiazole (0.86 g, 3.2 mmol, 0.93 eq.) portionwise. The mixture was stirred for further 5 mins before removal of the cooling bath and continued at ambient temperature. LCMS after 2 h would indicate reaction complete. MeCN was evaporated and the residue was purified by chromatography on silica gel to yield N-[(2-bromo-1,3-thiazol-4-yl)methoxy]-1-(1-methyl-1H-tetrazol-5-yl)-1-phenylmethanimine (6.9 g, 79% yield, 9:1 mixture of stereoisomers).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08557849B2 |
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| 출처 데이터셋 | uspto-grants-2013_10 |
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| ORD ID | ord-263d67cf9e924700af90064f0277fc34 |
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| 출처 메모 | uspto-grants-2013_10 |
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