Tetrahydrofuran → HCID 178473153, Verbindung

HRID 731427Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 731427
[CH2:1]([O:3][C:4](=[O:13])[CH2:5][S:6][C:7]1[S:11][C:10]([NH2:12])=[N:9][CH:8]=1)[CH3:2].[CH:14]1([NH:19][C@H:20]2[CH2:25][CH2:24][C@H:23]([CH2:26][CH3:27])[CH2:22][CH2:21]2)[CH2:18][CH2:17][CH2:16][CH2:15]1.C1C[O:31][CH2:30]C1>CN(C1C=CN=CC=1)C>[CH2:1]([O:3][C:4](=[O:13])[CH2:5][S:6][C:7]1[S:11][C:10]([NH:12][C:30]([N:19]([CH:14]2[CH2:15][CH2:16][CH2:17][CH2:18]2)[C@H:20]2[CH2:21][CH2:22][C@H:23]([CH2:26][CH3:27])[CH2:24][CH2:25]2)=[O:31])=[N:9][CH:8]=1)[CH3:2]

Komponenten

5

Edukt 3

HCID 8028TetrahydrofuranHCID 21455623Ethyl 2-(2-aminothiazol-5-ylthio)acetateHCID 178455796HCID 178455796, Verbindung

Produkt 1

HCID 178473153HCID 178473153, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 142844-(Dimethylamino)pyridineKatalysator

Reaktionsbedingungen

Temperatur
55 °C

Versuchsvorschrift

An equimolar mixture of 1,1-carbonyldiimidazole, (2-amino-thiazol-5-ylsulfanyl)-acetic acid ethyl ester and DMAP (5 mol %) in THF was heated for 5 h at 50-60° C. and then cooled to room temperature. Then cyclopentyl-(trans-4-ethyl-cyclohexyl)-amine (1 equivalent; see Step 2) was added and the reaction is stirred overnight at room temperature. The reaction mixture was quenched with water. The organic phase was isolated and the aqueous phase was extracted with CH2Cl2, and the combined organic phases were dried and concentrated in vacuo. The crude product was dissolved in MeCN and purified (HPLC method 1) to give {2-[3-cyclopentyl-3-(trans-4-ethyl-cyclohexyl)-ureido]-thiazol-5-ylsulfanyl}-acetic acid ethyl ester. This material was dissolved in MeOH and treated with 15 equivalents of 1N NaOH over night at room temperature. MeOH was removed by evaporation. Addition of 1N HCl to pH<1 caused precipitation. The precipitate was isolated by filtration, washed with water and dried to give the title compound.

Aufarbeitung

  1. temperaturecooled to room temperature
  2. customThe reaction mixture was quenched with water
  3. customThe organic phase was isolated
  4. extractionthe aqueous phase was extracted with CH2Cl2
  5. customthe combined organic phases were dried
  6. concentrationconcentrated in vacuo
  7. dissolutionThe crude product was dissolved in MeCN
  8. custompurified (HPLC method 1)

Quellen und Nachweise

ORD-Eintrag
ord-0be453f4d059478fb8f472bd8960cdae
Quelldatensatz
uspto-grants-2009_09
Patentnummer
US07582769B2

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