反应详情

The (2-methyl-2′-methoxy-[1,1′-biphenyl]-4-yl)carboxylic acid of Step B (0.50 g, 2.06 mmol) was suspended in thionyl chloride (3 mL) and the mixture heated at reflux for 30 minutes. After cooling, the thionyl chloride was removed in vacuo. The residue was dissolved in toluene and concentrated in vacuo to give the crude acid chloride as a brown oil. The acid chloride was then dissolved in dichloromethane (5 mL) and slowly added to a solution of 10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine (0.57 g, 3.10 mmol) and N,N-diisopropylethyl amine (0.79 mL, 4.53 mmol) in dichloromethane (15 mL). After stirring for 1 hour, the reaction was quenched with water. The organic layer was washed with 1 N hydrochloric acid, 1 N sodium hydroxide and brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to give a yellow foam. Purification by flash chromatography using a solvent gradient of 5 to 15% ethyl acetate in hexane yielded a white foam which crystallized upon sonication in ethanol/hexane to give 0.42 g of the desired title product as a white solid, m.p. 133–135° C.

1. temperaturethe mixture heated
2. temperatureat reflux for 30 minutes
3. temperatureAfter cooling
4. customthe thionyl chloride was removed in vacuo
5. dissolutionThe residue was dissolved in toluene
6. concentrationconcentrated in vacuo
7. customto give the crude acid chloride as a brown oil
8. customthe reaction was quenched with water
9. washThe organic layer was washed with 1 N hydrochloric acid, 1 N sodium hydroxide and brine
10. dry with materialdried over anhydrous sodium sulfate
11. filtrationfiltered
12. concentrationconcentrated in vacuo
13. customto give a yellow foam
14. customPurification by flash chromatography
15. customyielded a white foam which
16. customcrystallized upon sonication in ethanol/hexane