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Ammonia → 1,3,5-Triethyl-4-(1H-imidazol-2-ylmethyl)-1H-pyrazole

HRID 254584
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HRID 254584 반응식
C([N:8]1[CH:12]=[CH:11][N:10]=[C:9]1[CH2:13][C:14]1[C:15]([CH2:23][CH3:24])=[N:16][N:17]([CH2:21][CH3:22])[C:18]=1[CH2:19][CH3:20])C1C=CC=CC=1.[Na].N>>[CH2:21]([N:17]1[C:18]([CH2:19][CH3:20])=[C:14]([CH2:13][C:9]2[NH:8][CH:12]=[CH:11][N:10]=2)[C:15]([CH2:23][CH3:24])=[N:16]1)[CH3:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 222AmmoniaHCID 5360545SodiumHCID 589518964-(1-Benzyl-1H-imidazol-2-ylmethyl)-1,3,5-triethyl-1H-pyrazole

생성물 1

HCID 589518391,3,5-Triethyl-4-(1H-imidazol-2-ylmethyl)-1H-pyrazole

실험 절차

1,3,5-Triethyl-4-(1H-imidazol-2-ylmethyl)-1H-pyrazole was prepared from 4-(1-benzyl-1H-imidazol-2-ylmethyl)-1,3,5-triethyl-1H-pyrazole by debenzylation with sodium in liquid ammonia for 10 min. The blue reaction mixture was quenched by addition of solid ammonium chloride, the ammonia evaporated and the residue distributed between water and t-butyl methyl ether. The organic phase was washed with brine, dried over sodium sulfate, filtered and evaporated. 1,3,5-Triethyl-4-(1H-imidazol-2-ylmethyl)-1H-pyrazole was obtained as light yellow viscous oil; MS (ISP): 233.0 ((M+H)+.).

후처리

  1. customThe blue reaction mixture
  2. customwas quenched by addition of solid ammonium chloride
  3. customthe ammonia evaporated
  4. washThe organic phase was washed with brine
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. customevaporated

출처 및 근거

ORD 기록
ord-84efac272045442f8e800e3780470cc0
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07875645B2

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