تفاعل #710477

ord-e0110b7b7b7a4c6ba457b86c8afcb6fd

معادلة التفاعل

O
water
Cl.N=c1ccccn1Cc1ccc(Cl)nc1
1-[(6-chloropyridin-3-yl)methyl]pyridin-2(1H)-imine hydrochloride
CCN(CC)CC
triethylamine
O=C(Cl)C(Cl)(Cl)Cl
trichloroacetyl chloride
O
water
O=C(N=c1ccccn1Cc1ccc(Cl)nc1)C(Cl)(Cl)Cl
2,2,2-trichloro-N-[1-((6-chloropyridin-3-yl)methyl)pyridin-2(1H)-ylidene]-acetamide
المردود 62.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe reaction and liquid separation
  2. 2
    غسيلThe organic layer was washed once with water and twice with 1% hydrochloric acid
  3. 3
    تجفيفdried over anhydrous magnesium sulfate
  4. 4
    تركيزconcentrated under reduced pressure
  5. 5
    workup.ADDITIONDiethyl ether was added
  6. 6
    أخرىto precipitate a solid
  7. 7
    أخرىthus the solid was collected
  8. 8
    أخرىdried
  9. 9
    أخرىto obtain the subject material
  10. 10
    أخرىAmount obtained 61 mg (yield 62%)

الإجراء التجريبي

70 mg (0.27 mmol) of the 1-[(6-chloropyridin-3-yl)methyl]pyridin-2(1H)-imine hydrochloride obtained by the method described in another method of Synthetic Example P1 was dissolved in 4 ml of anhydrous dichloromethane, 94 μl (0.68 mmol, 68 mg) of triethylamine and 33 g (0.27 mmol, 49 mg) of trichloroacetyl chloride were added thereto in sequence, and the resulting mixture was stirred at room temperature for 1 hour. After the reaction was completed, water was added thereto to stop the reaction and liquid separation was performed with dichloromethane and water. The organic layer was washed once with water and twice with 1% hydrochloric acid, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. Diethyl ether was added thereto to precipitate a solid, and thus the solid was collected and dried to obtain the subject material. Amount obtained 61 mg (yield 62%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09301525B2uspto-grants-2016_04