تفاعل #8342

ord-8a78da593f264a14928d76c76ca79538

معادلة التفاعل

[C]=O
carbon monoxide
CC(=O)[O-].[Na+]
sodium acetate
ClCCl
CH2Cl2
Brc1ccc2nccc(-c3c(-c4ccccn4)nn4c3CCC4)c2c1
6-bromo-4-(2-pyridin-2-yl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)-quinoline
COC(=O)c1ccc2nccc(-c3c(-c4ccccn4)nn4c3CCC4)c2c1
4-(2-Pyridin-2-yl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)-quinoline-6-carboxylic acid methyl ester

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture is cooled
  2. 2
    ترشيحfiltered
  3. 3
    تركيزconcentrated in vacuo
  4. 4
    أخرىThe product is partitioned between ethyl acetate
  5. 5
    تجفيفThe organic layer is dried over sodium sulfate
  6. 6
    تركيزconcentrated in vacuo
  7. 7
    أخرىThe residue is chromatographed on SiO2 (dichloromethane to 2% methanol/dichloromethane)
  8. 8
    أخرىto yield a solid, 918 mg (97%)

الإجراء التجريبي

To a mixture of sodium acetate (0.84 g, 10.2 mmol) and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II):CH2Cl2 (42 mg, 0.05 mmol) in methanol (40 mL) is added 6-bromo-4-(2-pyridin-2-yl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)-quinoline (1.0 g, 2.56 mmol). The mixture is heated at 90° C. under 68 psi carbon monoxide for 24 h. The mixture is cooled, filtered, and concentrated in vacuo. The product is partitioned between ethyl acetate and: water. The organic layer is dried over sodium sulfate and concentrated in vacuo. The residue is chromatographed on SiO2 (dichloromethane to 2% methanol/dichloromethane) to yield a solid, 918 mg (97%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07087626B2uspto-grants-2006_08