تفاعل #84122

ord-4326d0e723154975bf57625f2b7dd4b3

الكواشف

لا شيء

ظروف التفاعل

درجة الحرارة
30°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThen the mixture was heated to 65° C. for 1.5 hours
  2. 2
    أخرىThe mixture was quenched with ice-water (100 mL)
  3. 3
    ترشيحThe mixture was filtered off
  4. 4
    استخلاصthe filtrate was extracted with EtOAc (50 mL×3)
  5. 5
    غسيلthe organic layer was washed with brine (100 mL)
  6. 6
    تجفيفdried over Na2SO4
  7. 7
    تركيزconcentrated in vacuo
  8. 8
    أخرىPurification by column chromatography on silica gel (PE/EtOAc=15/1)

الإجراء التجريبي

A solution of 2-chloro-6-methoxyquinolin-4-amine (4.50 g, 21.6 mmol) in HF-pyridine (45 mL) was cooled to −10-0° C. Then NaNO2(1.80 g, 26.1 mmol) was added portionwise and the mixture was stirred at 0° C. for 1 hour and at 30° C. for 1 hour. Then the mixture was heated to 65° C. for 1.5 hours. The mixture was quenched with ice-water (100 mL); the aqueous layer was neutralized with 2 M NaOH to pH 7. The mixture was filtered off and the filtrate was extracted with EtOAc (50 mL×3), the organic layer was washed with brine (100 mL), dried over Na2SO4 and concentrated in vacuo. Purification by column chromatography on silica gel (PE/EtOAc=15/1) gave Intermediate 7 (3.60 g, yield: 40%). 1H NMR (CDCl3 400 MHz): δ 7.92 (dd, J=9.2, 1.6 Hz, 1H), 7.40 (dd, J=9.2, 2.8 Hz, 1H), 7.25 (s, 1H), 7.10 (d, J=9.2 Hz, 1H), 3.97 (s, 3H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09433618B2uspto-grants-2016_09