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Azetidine → 2-{4-[4-(Azetidin-1-ylacetyl)piperazin-1-yl]anilino}-4-(1-isopropyl-2-methyl-1H-imidazol-5-yl)pyrimidine hydrochloride

HRID 1441312
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1441312
[Cl:1][CH2:2][C:3]([N:5]1[CH2:10][CH2:9][N:8]([C:11]2[CH:32]=[CH:31][C:14]([NH:15][C:16]3[N:21]=[C:20]([C:22]4[N:26]([CH:27]([CH3:29])[CH3:28])[C:25]([CH3:30])=[N:24][CH:23]=4)[CH:19]=[CH:18][N:17]=3)=[CH:13][CH:12]=2)[CH2:7][CH2:6]1)=[O:4].[NH:33]1[CH2:36][CH2:35][CH2:34]1>CCOC(C)=O>[ClH:1].[N:33]1([CH2:2][C:3]([N:5]2[CH2:10][CH2:9][N:8]([C:11]3[CH:32]=[CH:31][C:14]([NH:15][C:16]4[N:21]=[C:20]([C:22]5[N:26]([CH:27]([CH3:29])[CH3:28])[C:25]([CH3:30])=[N:24][CH:23]=5)[CH:19]=[CH:18][N:17]=4)=[CH:13][CH:12]=3)[CH2:7][CH2:6]2)=[O:4])[CH2:36][CH2:35][CH2:34]1
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Komponenten

4

Edukt 2

HCID 10422AzetidineHCID 114765422-{4-[4-(Chloroacetyl)piperazin-1-yl]anilino}-4-(1-isopropyl-2-methyl-1H-imidazol-5-yl)pyrimidine

Produkt 1

HCID 686870802-{4-[4-(Azetidin-1-ylacetyl)piperazin-1-yl]anilino}-4-(1-isopropyl-2-methyl-1H-imidazol-5-yl)pyrimidine hydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

2-{4-[4-(Chloroacetyl)piperazin-1-yl]anilino}-4-(1-isopropyl-2-methyl-1H-imidazol-5-yl)pyrimidine (Example 24; 0.34 g, 0.75 mmol) and azetidine (2 ml) was stirred for 24 hours at ambient temperature. The solution was diluted with EtOAc (20 ml), washed with aqueous saturated sodium bicarbonate solution (10 ml) and aqueous saturated sodium chloride solution (10 ml), then dried and evaporated at reduced pressure. The residue was purified by chromatography on a 40 g silica column, eluted with a 3% MeOH-ammonia/DCM to 5% MeOH-ammonia/DCM gradient, to give the amine, which was converted to the hydrochloride salt by dissolving in EtOAc (3 ml) and treating with a 1.0 molar solution of ethereal-HCl (0.75 ml). The solid was triturated with ether (20 ml) and filtered to give the title compound (24 mg, 7%). NMR: 9.77 (s, 1H), 8.58 (d, 1H), 8.20 (s, 1H), 7.61 (d, 2H), 7.35-7.24 (m, 2H), 7.13 (d, 1H), 5.64-5.55 (m, 1H), 4.65 (brs, 1H), 4.44 (d, 2H), 4.23-4.11 (m, 2H), 4.09-3.96 (m, 2H), 3.81-3.71 (m, 2H), 3.69-3.59 (m, 2H), 3.42-3.31 (m, 2H), 3.30-3.17 (m, 2H), 2.48-2.24 (m, 2H), 2.81 (s, 3H), 1.48 (d, 6H); m/z 475.

Aufarbeitung

  1. washwashed with aqueous saturated sodium bicarbonate solution (10 ml) and aqueous saturated sodium chloride solution (10 ml)
  2. customdried
  3. customevaporated at reduced pressure
  4. customThe residue was purified by chromatography on a 40 g silica column
  5. washeluted with a 3% MeOH-ammonia/DCM to 5% MeOH-ammonia/DCM gradient

Quellen und Nachweise

ORD-Eintrag
ord-80d5bf070b374f459603190997795210
Quelldatensatz
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07655652B2

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