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1H-1,2,4-Triazole → HCID 13650454, 화합물

HRID 1761889
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HRID 1761889 반응식
[NH:1]1[CH:5]=[N:4][CH:3]=[N:2]1.C(=O)([O-])[O-].[K+].[K+].[C:12]1([C:18]2[CH:23]=[CH:22][C:21]([C:24]([CH:26](Br)[CH2:27][CH2:28]Cl)=[O:25])=[CH:20][CH:19]=2)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>C(#N)C>[N:1]1([C:26]2([C:24]([C:21]3[CH:22]=[CH:23][C:18]([C:12]4[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=4)=[CH:19][CH:20]=3)=[O:25])[CH2:28][CH2:27]2)[CH:5]=[N:4][CH:3]=[N:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 92571H-1,2,4-TriazoleHCID 11430Potassium CarbonateHCID 14125892HCID 14125892, 화합물

생성물 1

HCID 13650454HCID 13650454, 화합물

시약·촉매·용매 1

HCID 6342Acetonitrile용매2회

실험 절차

44.7 g (0.648 mol) of 1,2,4-triazole and 89.5 g (0.648 mol) of anhydrous potassium carbonate were suspended in 525 ml of acetonitrile, and, under reflux, 202 g (0.6 mol) of of acetonitrile, and, under reflux, 202 g (0.6 mol) of 1-bromo-3-chloropropyl 4-phenylphenyl ketone were added in portions over 20 minutes. After a reaction time of 3 hours under reflux, the mixture was poured into ice water and the crystals obtained were filtered off under suction. 162.0 g (93% of theory) of colorless crystals of melting point 154°-5° C. were obtained.

후처리

  1. temperatureunder reflux
  2. temperatureAfter a reaction time of 3 hours under reflux
  3. customthe crystals obtained
  4. filtrationwere filtered off under suction
  5. custom162.0 g (93% of theory) of colorless crystals of melting point 154°-5° C. were obtained

출처 및 근거

ORD 기록
ord-c0576bb4dcea473386e512fd4a1db6a2
출처 데이터셋
uspto-grants-1989_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04829075

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