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Water → 3-[2-(4-Anilinocarbonylmethylamino-1-piperidyl) ethyl]indole

HRID 442481
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HRID 442481 반응식
O.[NH2:2][CH:3]1[CH2:8][CH2:7][N:6]([CH2:9][CH2:10][C:11]2[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[NH:13][CH:12]=2)[CH2:5][CH2:4]1.C(N(CC)CC)C.Cl[CH2:28][C:29]([NH:31][C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1)=[O:30].O>CN(C)C=O>[NH:31]([C:29]([CH2:28][NH:2][CH:3]1[CH2:8][CH2:7][N:6]([CH2:9][CH2:10][C:11]2[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[NH:13][CH:12]=2)[CH2:5][CH2:4]1)=[O:30])[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 8471TriethylamineHCID 11485ChloroacetanilideHCID 203843533-[2-(4-Aminopiperidyl)ethyl]indole, hydrate

생성물 1

HCID 542686533-[2-(4-Anilinocarbonylmethylamino-1-piperidyl) ethyl]indole수율 109.2%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

실험 절차

3-[2-(4-Amino-1-piperidyl) ethyl]indole hydrate (1.31g.) was dissolved in dimethylformamide (15 ml) containing triethylamine (2 ml) and chloroacetanilide (0.85g) added. The mixture was stirred for 24 hours, poured into water (100 ml) and extracted with chloroform (2 × 50 ml). The combined chloroform layers were washed with water, dried (MgSO4), filtered and evaporated to give the title compound as an amber oil (2.06 g). This was converted to the hydrochloride (1.29 g), m.p. 240.7°, on addition of EtOH-HC1 and Et2O.

후처리

  1. additionadded
  2. extractionextracted with chloroform (2 × 50 ml)
  3. washThe combined chloroform layers were washed with water
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. customevaporated

출처 및 근거

ORD 기록
ord-02982ff8c946439b80372bd23b5e340d
출처 데이터셋
uspto-grants-1977_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04045566

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