تفاعل #41261

ord-d13f1c111a6a4d28ac8fdd786615866a

معادلة التفاعل

O=C1CCC=NN1c1ccc(-c2ccc(Br)cc2)cc1
2-(4′-bromobiphenyl-4-yl)-4,5-dihydropyridazin-3(2H)-one
CN1C[C@H]2CCN[C@H]2C1.Cl.Cl
(3aR,6aR)-5-methylhexahydropyrrolo[3,4-b]pyrrole dihydrochloride
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
CN(C)c1ccccc1-c1ccccc1P(C1CCCCC1)C1CCCCC1
2-dicyclohexylphosphino-2′(N,N-dimethylamino)biphenyl
CN1C[C@H]2CCN(c3ccc(-c4ccc(N5N=CCCC5=O)cc4)cc3)[C@H]2C1
title compound
المردود 15.6%
CN1C[C@H]2CCN(c3ccc(-c4ccc(N5N=CCCC5=O)cc4)cc3)[C@H]2C1
2-{4′-[(3aR,6aR)-5-Methylhexahydropyrrolo[3,4-b]pyrrol-1(2H)-yl]biphenyl-4-yl}-4,5-dihydropyridazin-3(2H)-one
المردود 15.6%

المذيبات

ظروف التفاعل

درجة الحرارة
100°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىA small pressure tube equipped with a magnetic stir bar
  2. 2
    أخرىpurging with argon the tube
  3. 3
    أخرىCrude product was purified by flash chromatography (silica gel, gradient 2 to 10% methanol in dichloromethane), which

الإجراء التجريبي

A small pressure tube equipped with a magnetic stir bar was charged with 100 mg of 2-(4′-bromobiphenyl-4-yl)-4,5-dihydropyridazin-3(2H)-one, 58 mg of (3aR,6aR)-5-methylhexahydropyrrolo[3,4-b]pyrrole dihydrochloride, 350 mg of cesium carbonate, 15 mg of silver triflate, 4.2 mg of tris(dibenzylideneacetone)dipalladium, and 7.2 mg of 2-dicyclohexylphosphino-2′(N,N-dimethylamino)biphenyl and 2 ml of toluene. After sealing and purging with argon the tube was heated at 100° C. for 20 hours. Crude product was purified by flash chromatography (silica gel, gradient 2 to 10% methanol in dichloromethane), which yielded 17 mg of the title compound as a dark yellow oil. Mass spectroscopy gave (M+H)+ m/z 375.2, consistent with assigned structure.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07728031B2uspto-grants-2010_06