Amantadine → N-(Adamantan-1-yl)prop-2-enimidic acid

HRID 1614532

반응식

HRID 1614532 반응식
[C:1](Cl)(=[O:4])[CH:2]=[CH2:3].[C:6]12([NH2:16])[CH2:15][CH:10]3[CH2:11][CH:12]([CH2:14][CH:8]([CH2:9]3)[CH2:7]1)[CH2:13]2.C(N(CC)CC)C>C(OCC)C>[C:6]12([NH:16][C:1](=[O:4])[CH:2]=[CH2:3])[CH2:13][CH:12]3[CH2:11][CH:10]([CH2:9][CH:8]([CH2:14]3)[CH2:7]1)[CH2:15]2

참가 물질

5

실험 절차

A solution of acryloyl chloride (4.05 ml, 0.05 mole) in ethyl ether (25 ml) was added to a cold (+5° C.) solution of 1-adamantaneamine (7.65 g, 0.05 mole) and triethylamine (15.3 ml, 0.11 mole) in ethyl ether (300 ml) and the solution stirred for 72 hours at room temperature. The solvent was removed on a rotary evaporator. The residue was dissoled in ethyl acetate (100 ml), washed with 10 percent hydrochloric acid (100 ml) and water (50 ml), dried over sodium sulfate, filtered and the solvent removed in vacuo leaving an oily solid which was crystallized from methanol-ethyl acetate-hexane. The structure was confirmed by NMR.

후처리

  1. customThe solvent was removed on a rotary evaporator
  2. washwashed with 10 percent hydrochloric acid (100 ml) and water (50 ml)
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. customthe solvent removed in vacuo
  6. customleaving an oily solid which
  7. customwas crystallized from methanol-ethyl acetate-hexane

출처 및 근거

ORD 기록
ord-7ad86533a3154410807414295786aac6
출처 데이터셋
uspto-grants-1993_03
특허 번호
US05198435

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