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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11125생성일: 2026년 10월 26일

Azido(trimethyl)stannane → HCID 178418841, 화합물

https://huagongshe.com/reaction/11125

반응식

참여 물질

역할이름HCID투입량
반응물Azido(trimethyl)stannaneHCID 5104973—
반응물3-(4-(2-Chlorophenyl)-9-hydroxy-1,3-dioxo-2,3-dihydropyrrolo[3,4-c]carbazol-6(1H)-yl)propanenitrileHCID 24884697—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
용매Dimethylformamide tolueneHCID 21735183—
생성물HCID 178418841HCID 17841884172.2%

반응 단계

To a solution of nitrile (238) (0.68 g, 1.63 mmol) prepared as described in example 98 in toluene/dimethylformamide (5:1, 120 mL) was added azidotrimethyl tin (0.67 g, 3.26 mmol). The resulting solution was heated at reflux for 24 hours before a further portion of azidotrimethyl tin (0.34 g, 1.63 mmol) was added. After a further 24 hours at reflux the reaction was diluted with water and extraction with ethyl acetate. The organic phase was dried, the drying agent was removed and the solution was concentrated to dryness. Chromatography on silica eluting with ethyl acetatelhexane (3:1) to ethyl acetate/methanol (9:1), followed by crystallization from ethyl acetate/hexane, gave tetrazole (272) (0.54 g, 72%) as an orange powder, mp 230–234° C. (dec). 1H NMR δ [(CD3)2SO] 11.06 (br s, 1H), 9.37 (br s, 1H), 8.36 (d, J=2.4 Hz, 1H), 7.61 (s, 1H), 7.56 (m, 1H), 7.48 (m, 4H), 7.10 (dd, J=8.8, 2.4 Hz, 1H), 4.82 (t, J=6.9 Hz, 2H), 3.32 (obscured t, J=6.9 Hz, 2H). Found: C, 52.69; H, 4.05; N, 15.91. C23H15ClN6O3.31/2H2O requires: C, 52.93; H, 4.25; N, 16.09.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094798B1
출처 데이터셋uspto-grants-2006_08
ORD IDord-48da5ed2f8704646a3a54504d181f110
출처 메모uspto-grants-2006_08