Ammonia → 1-(2-Hydroxyethyl)-3-[2-(2,2,2-trifluoroethyl)guanidino]pyrazole

HRID 2291331노트

반응식

HRID 2291331 반응식
[OH:1][CH2:2][CH2:3][N:4]1[CH:8]=[CH:7][C:6]([NH:9][C:10]([NH:12][CH2:13][C:14]([F:17])([F:16])[F:15])=S)=[N:5]1.[NH3:18]>CCO>[OH:1][CH2:2][CH2:3][N:4]1[CH:8]=[CH:7][C:6]([NH:9][C:10]([NH2:18])=[N:12][CH2:13][C:14]([F:17])([F:16])[F:15])=[N:5]1

참가 물질

4

반응물 2

HCID 222AmmoniaHCID 543739781-(2-Hydroxyethyl)-3-[3-(2,2,2-trifluoroethyl)thioureido]pyrazole

생성물 1

HCID 212798481-(2-Hydroxyethyl)-3-[2-(2,2,2-trifluoroethyl)guanidino]pyrazole수율 99%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 1-(2-hydroxyethyl)-3-[3-(2,2,2-trifluoroethyl)thioureido]pyrazole (20.0 g.) in 5N ammonia in EtOH solution (700 ml.) was added yellow mercuric oxide (64.8 g.) with stirring. Stirring was continued for a period of 2 hours. The mixture was filtered through diatomaceous earth and the solvent then evaporated to dryness in vacuo. The residual oil was triturated with ether to give 1-(2-hydroxyethyl)-3-[2-(2,2,2-trifluoroethyl)guanidino]pyrazole (18.5 g.; 99%), m.p. 82°.

후처리

  1. stirringStirring
  2. filtrationThe mixture was filtered through diatomaceous earth
  3. customthe solvent then evaporated to dryness in vacuo
  4. customThe residual oil was triturated with ether

출처 및 근거

ORD 기록
ord-3de9a24170f142f390168fe5969e2d72
출처 데이터셋
uspto-grants-1989_01
특허 번호
US04795755

반응 노트

불러오는 중…