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Hydrochloric Acid → 5-(2-Aminomethylpropan-2-yl)-2-(4-methylphenyl)benzimidazole

HRID 1639140
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인쇄 미리보기

반응식

HRID 1639140 반응식
C([NH:4][CH2:5][C:6]([C:9]1[CH:24]=[CH:23][C:12]2[N:13]=[C:14]([C:16]3[CH:21]=[CH:20][C:19]([CH3:22])=[CH:18][CH:17]=3)[NH:15][C:11]=2[CH:10]=1)([CH3:8])[CH3:7])(=O)C.Cl>C(O)C>[NH2:4][CH2:5][C:6]([C:9]1[CH:24]=[CH:23][C:12]2[N:13]=[C:14]([C:16]3[CH:17]=[CH:18][C:19]([CH3:22])=[CH:20][CH:21]=3)[NH:15][C:11]=2[CH:10]=1)([CH3:8])[CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 198404055-(2-Acetamidomethyl-propan-2-yl)-2-(4-methylphenyl)benzimidazole

생성물 1

HCID 198403365-(2-Aminomethylpropan-2-yl)-2-(4-methylphenyl)benzimidazole

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

1.45 g. of the compound prepared in Example 26 is boiled under reflux for 48 hours in 35 ml. ethanol and 35 ml. concentrated hydrochloric acid. The solvent is removed in a vacuum and the residue is dissolved in water and neutralised with 2N aqueous ammonia solution. The substance which precipitates out is filtered off with suction. There is obtained 1.1 g. of the title compound; m.p. 45°-48° C.

후처리

  1. temperatureunder reflux for 48 hours in 35 ml
  2. customThe solvent is removed in a vacuum
  3. dissolutionthe residue is dissolved in water and neutralised with 2N aqueous ammonia solution
  4. customThe substance which precipitates out
  5. filtrationis filtered off with suction
  6. customThere is obtained 1.1 g

출처 및 근거

ORD 기록
ord-463b7beee1104ab38f9077f08caa4c2f
출처 데이터셋
uspto-grants-1989_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04882342

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