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HRID 726666생성일: 2026년 10월 25일

4-Toluenesulfonyl chloride → 6-Methylpyridazine-3-carbonitrile

https://huagongshe.com/reaction/726666

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물3-MethylpyridazineHCID 74208—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물Trimethylsilyl cyanideHCID 82115—
촉매Aluminum(III) ChlorideHCID 6451240—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물6-Methylpyridazine-3-carbonitrileHCID 1364294164%

반응 단계

To a stirring solution of 3-methylpyridazine (11 g, 118 mmol) in dichloromethane (200 mL) was added AlCl3 (0.05 g) followed by trimethylsilylcyanide (21 g, 211 mmol). After 20 min, a solution of p-toluenesulfonyl chloride (38 g, 201 mmol) in dichloromethane (50 mL) was added via addition funnel and the solution continued to stir overnight. The next morning, the solvent was removed in vacuo and the residue was suspended in ethanol with stirring for 15 min and then filtered to give a white solid. The solid was dissolved in tetrahydrofuran (200 mL) and to this stirring solution was added 1,8-diazabicyclo[5.4.0]undec-7-ene (16 mL, 105 mmol). After 1 h, the solvent was removed in vacuo and the residue was partitioned between hexanes and saturated aqueous NH4Cl. The phases were separated and the aqueous phase was basified with solid Na2CO3, then extracted three times with ethyl acetate. The combined ethyl acetate phases were dried (MgSO4), filtered and concentrated in vacuo to give 9 g (64%) of white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05710130
출처 데이터셋uspto-grants-1998_01
ORD IDord-7e3590ad24c1453da52a2934999d7762
출처 메모uspto-grants-1998_01