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M-Cresol → HCID 178433662, 화합물

HRID 1862841
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HRID 1862841 반응식
Cl.Cl.[CH3:3][C:4]1[NH:8][CH:7]=[N:6][C:5]=1[CH2:9][CH2:10][NH2:11].[OH-].[Na+].C1(C)C=CC=C(O[C:21](=[NH:25])[NH:22][C:23]#[N:24])C=1.C1C(O)=CC=CC=1C>C(O)(C)C>[C:21]([NH:22][C:23]([NH:11][CH2:10][CH2:9][C:5]1[N:6]=[CH:7][NH:8][C:4]=1[CH3:3])=[NH:24])#[N:25]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 342M-CresolHCID 14798Sodium HydroxideHCID 2158192-(5-methyl-1H-imidazol-4-yl)ethan-1-amine dihydrochlorideHCID 178425733HCID 178425733, 화합물

생성물 1

HCID 178433662HCID 178433662, 화합물

시약·촉매·용매 1

HCID 3776Isopropanol용매

실험 절차

4.94 g. (0.249 mole) 5-methyl-4-(2-aminoethyl) imidazole dihydrochloride is converted to the free base with NaOH. The free base is combined with 4.36 g. (0.0249 mole) of O-m-tolyl-N-cyanoisourea in 63 ml. isopropanol. This mixture is refluxed for one hour. The mixture is then cooled to room temperature, filtered to remove insoluble material, and the solvent is evaporated to obtain a cloudy oil of the product mixed with m-cresol.

후처리

  1. temperatureThis mixture is refluxed for one hour
  2. filtrationfiltered
  3. customto remove insoluble material
  4. customthe solvent is evaporated
  5. customto obtain a cloudy oil of the product

출처 및 근거

ORD 기록
ord-e42112a5cade4e968931eb96eaf9b353
출처 데이터셋
uspto-grants-1979_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04166860

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