4-Benzylpiperidine → HCID 69420844, Verbindung

HRID 1357043Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1357043
[CH3:1][O:2][C:3]1[C:4]([C:12]([OH:14])=O)=[CH:5][C:6]2[NH:10][CH:9]=[N:8][C:7]=2[CH:11]=1.CC[N:17]=C=NCCCN(C)C.Cl.[CH2:27]([CH:34]1[CH2:39][CH2:38][NH:37][CH2:36][CH2:35]1)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>CN(C1C=CN=CC=1)C.CN(C=O)C.C(Cl)Cl>[CH3:1][O:2][C:3]1[C:4]([C:12]([NH2:17])=[O:14])=[CH:5][C:6]2[NH:10][C:9]([N:37]3[CH2:38][CH2:39][CH:34]([CH2:27][C:28]4[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=4)[CH2:35][CH2:36]3)=[N:8][C:7]=2[CH:11]=1

Komponenten

6

Versuchsvorschrift

6-methoxy-5-benzimidazole carboxylic acid, (1 equivalent) was treated with 1.1 equivalent of EDAC.HCl and 1 equivalent of 4-benzylpiperidine in the presence of a catalytic amount of DMAP in DMF/DCM 1:1 for 3-6 hrs. The reaction mixture was then concentrated and taken up in ethyl acetate. After washing with 5% aq. Sodium carbonate and a solution of saturated sodium chloride, the organic layer was dried over anhydrous sodium sulfate and concentrated to give crude material. This crude material was purified by chromatography on silica. M+ 349, Exp. 349.

Aufarbeitung

  1. concentrationThe reaction mixture was then concentrated
  2. washAfter washing with 5% aq. Sodium carbonate
  3. dry with materiala solution of saturated sodium chloride, the organic layer was dried over anhydrous sodium sulfate
  4. concentrationconcentrated
  5. customto give crude material
  6. customThis crude material was purified by chromatography on silica

Quellen und Nachweise

ORD-Eintrag
ord-e3a26c0ff6f34920b9bbea0de0aa0ed9
Quelldatensatz
uspto-grants-2003_07
Patentnummer
US06589954B1

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