1,1'-Carbonyldiimidazole → N-[2-(3,4-Dichlorophenyl)-2-(4-hydroxy-4-phenyl-piperidino)ethyl]-N-methyl-3,5-bis(trifluoromethyl)phenylacetamide hydrochloride salt

HRID 609865Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 609865
[F:1][C:2]([F:18])([F:17])[C:3]1[CH:4]=[C:5]([CH2:13][C:14]([OH:16])=O)[CH:6]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:8]=1.C(N1C=CN=C1)(N1C=CN=C1)=O.[Cl:31][C:32]1[CH:33]=[C:34]([CH:39]([N:43]2[CH2:48][CH2:47][C:46]([OH:55])([C:49]3[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=3)[CH2:45][CH2:44]2)[CH2:40][NH:41][CH3:42])[CH:35]=[CH:36][C:37]=1[Cl:38]>O1CCCC1>[ClH:31].[Cl:31][C:32]1[CH:33]=[C:34]([CH:39]([N:43]2[CH2:44][CH2:45][C:46]([OH:55])([C:49]3[CH:50]=[CH:51][CH:52]=[CH:53][CH:54]=3)[CH2:47][CH2:48]2)[CH2:40][N:41]([CH3:42])[C:14](=[O:16])[CH2:13][C:5]2[CH:6]=[C:7]([C:9]([F:11])([F:12])[F:10])[CH:8]=[C:3]([C:2]([F:17])([F:18])[F:1])[CH:4]=2)[CH:35]=[CH:36][C:37]=1[Cl:38]

Komponenten

5

Edukt 3

HCID 682631,1'-CarbonyldiimidazoleHCID 1235873,5-Bis(trifluoromethyl)phenylacetic acidHCID 15434904HCID 15434904, Verbindung

Produkt 1

HCID 22129658N-[2-(3,4-Dichlorophenyl)-2-(4-hydroxy-4-phenyl-piperidino)ethyl]-N-methyl-3,5-bis(trifluoromethyl)phenylacetamide hydrochloride saltAusbeute 48 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Reaktionsbedingungen

Temperatur
23 °C

Versuchsvorschrift

A solution of 3,5-bis(trifluoromethyl)phenylacetic acid (1.61 g) and 1,1'-carbonyldiimidazole (1.01 g) in tetrahydrofuran (15 mL) was stirred at reflux for 0.5 hours. The reaction was cooled to 23° C. and treated with a solution of N-[2-(3,4-dichlorophenyl)-2-(4-hydroxy-4-phenylpiperdino)ethyl]methylamine (2.24 g) in tetrahydrofuran (70 mL). The reaction was stirred at 23° C. for 18 hours. The reaction was evaporated to an oil, and the oil was partitioned between diethylether and 1N hydrochloric acid (100 mL). The organic layer was treated with etheral hydrochloric acid to produce the title compound as a white solid (950 mg); mp 230° C.; MS: m/z=633(M+1); NMR: 1.73 (m,2), 2.42 (m,1), 2.75 (m,1), 3.01 (s,4), 3.86 (m,4,), 4.43 (m,1), 4.85 (m,1), 5.34 (m,1), 7.34 (m,5), 7.73 (s2), 7.87 (m,5), 8.06 (s,1), 11.36 (broad s,1). Analysis Calculated: C, 53.79; H, 4.36; N, 4.18; Found: C, 54.06; H, 4.48; N, 4.23.

Aufarbeitung

  1. temperatureat reflux for 0.5 hours
  2. customThe reaction was evaporated to an oil
  3. customthe oil was partitioned between diethylether and 1N hydrochloric acid (100 mL)
  4. additionThe organic layer was treated with etheral hydrochloric acid

Quellen und Nachweise

ORD-Eintrag
ord-62388616b5514758bb0b21a6dbd8050f
Quelldatensatz
uspto-grants-1999_12
Patentnummer
US05998444

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