Sodium Hydroxide → 6-(Trifluoromethyl)pyrazin-2-amine

HRID 971634노트

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HRID 971634 반응식
Br[CH:2](Br)[C:3](=O)[C:4]([F:7])([F:6])[F:5].C([O-])(=O)C.[Na+].Br.Br.[NH2:17][CH2:18][C:19]([NH2:21])=[NH:20].[OH-].[Na+]>O.CO>[NH2:21][C:19]1[CH:18]=[N:17][CH:2]=[C:3]([C:4]([F:7])([F:6])[F:5])[N:20]=1

참가 물질

7

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온도
20 °C

실험 절차

A mixture of 6.6 g. of 3,3-dibromo-1,1,1-trifluoropropanone, 60 ml. of water, and 6.6 g. sodium acetate was refluxed for about 10 minutes. The solution thus obtained was cooled and added dropwise to a solution of 6 g. of aminoacetamidine dihydrobromide in 90 ml. of methanol cooled to a temperature of about -30° C., followed by the addition of a solution of 3.6 g. of sodium hydroxide pellets in 25 ml. of water. The reaction mixture was stirred and warmed gradually to about 20° C. over a period of about two hours. The reaction product mixture was concentrated in vacuo to remove the methanol, and the residue extracted with ethyl acetate. There was obtained product weighing 3.6 g. and having a melting point of about 133°-136° C. after recrystallization from a mixture of benzene and hexane. The product was identified by NMR spectrum and elemental analyses as 2-amino-6-trifluoromethylpyrazine.

후처리

  1. additionA mixture of 6.6 g
  2. customThe solution thus obtained
  3. temperaturewas cooled
  4. additionadded dropwise to a solution of 6 g
  5. additionfollowed by the addition of a solution of 3.6 g
  6. concentrationThe reaction product mixture was concentrated in vacuo
  7. customto remove the methanol
  8. extractionthe residue extracted with ethyl acetate
  9. customThere was obtained product
  10. customafter recrystallization
  11. additionfrom a mixture of benzene and hexane

출처 및 근거

ORD 기록
ord-e995d15a1fc54fd9be66fa8282ce82c1
출처 데이터셋
uspto-grants-1979_07
특허 번호
US04160834

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