Sodium hydride → 3-(Aminomethyl)benzoic acid hydrochloride

HRID 49933

반응식

HRID 49933 반응식
[NH:1](C(OC(C)(C)C)=O)C(OC(C)(C)C)=O.[H-].[Na+].[Cl:18][CH2:19][C:20]1[CH:21]=[C:22]([CH:26]=[CH:27][CH:28]=1)[C:23]([OH:25])=[O:24]>CN(C)C=O>[ClH:18].[NH2:1][CH2:19][C:20]1[CH:21]=[C:22]([CH:26]=[CH:27][CH:28]=1)[C:23]([OH:25])=[O:24]

참가 물질

5

반응 조건

온도
80 °C

실험 절차

4.34 g (20.0 mmol) of di(t-butyl) iminodicarboxylate was added to a mixture of 800 mg (20.0 mmol) of sodium hydride (60% dispersion in mineral oil) and 50 ml of dimethylformamide. 1.71 g (10.0 mmol) of 3-chloromethylbenzoic acid was added to the obtained mixture, and they were stirred at 80° C. for 2 hours. After the concentration under reduced pressure, 40 ml of dioxane containing 4 M of hydrogen chloride was added to the residue, and they were stirred at room temperature overnight. A white precipitate thus formed was taken by the filtration and washed with ethyl acetate to obtain 3-aminomethylbenzoic acid hydrochloride as white crystals. A mixture of this aminomethyl compound, 10 ml of water, 10 ml of 28% aqueous ammonia and 3.00 g (71.4 mmol) of cyanamide was stirred at 60° C. for 7 days. The solvent was evaporated, and the residue was purified by the reversed-phase HPLC in the same manner as that in step 5 in Example 1 to obtain the title compound.

후처리

  1. concentrationAfter the concentration under reduced pressure, 40 ml of dioxane containing 4 M of hydrogen chloride
  2. additionwas added to the residue, and they
  3. stirringwere stirred at room temperature overnight
  4. customA white precipitate thus formed
  5. filtrationwas taken by the filtration
  6. washwashed with ethyl acetate

출처 및 근거

ORD 기록
ord-db7ee05540cf44fa9363b18f21aa4401
출처 데이터셋
uspto-grants-2004_03
특허 번호
US06710056B2

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