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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

반응식

참여 물질

역할이름HCID투입량
반응물1,5-Diazabicyclo(4.3.0)non-5-eneHCID 76349—
반응물2-Bromo-4-(1-bromoethyl)-1,3-thiazoleHCID 66860748—
반응물N-hydroxy-1-(1-methyl-1H-tetrazol-5-yl)-1-phenylmethanimineHCID 135990939—
용매AcetonitrileHCID 6342—
생성물N-[(2-bromo-1,3-thiazol-4-yl)methoxy]-1-(1-methyl-1H-tetrazol-5-yl)-1-phenylmethanimineHCID 86649974568.6%

반응 조건

온도0 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08557849B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-263d67cf9e924700af90064f0277fc34
출처 메모uspto-grants-2013_10