Reaktion #1973922

ord-1c27028976634010ba50d1885c017ffc

Reaktionsgleichung

O
water
CCOCn1c(-c2nc(Cl)ncc2Cl)cc2c(C(=O)NC3CC3)cccc21
N-cyclopropyl-2-(2,5-dichloropyrimidin-4-yl)-1-(ethoxymethyl)-1H-indole-4-carboxamide
Cl.N[C@@H]1CCC[C@H]1O
(1R,2R)-2-aminocyclopentanol hydrochloride
CCN(C(C)C)C(C)C
DIPEA
CCOCn1c(-c2nc(N[C@@H]3CCC[C@H]3O)ncc2Cl)cc2c(C(=O)NC3CC3)cccc21
2-{5-chloro-2-[(1R,2R)-2-hydroxycyclopentylamino]pyrimidin-4-yl}-N-cyclopropyl-1-(ethoxymethyl)-1H-indole-4-carboxamide
Ausbeute 93.6%

Lösungsmittel

Reaktionsbedingungen

Temperatur
80°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with EA (2×500 mL)
  2. 2
    WaschenThe combined extracts are washed with aqueous saturated sodium chloride (500 mL)
  3. 3
    Trocknendried over Na2SO4
  4. 4
    Einengenconcentrated in vacuo
  5. 5
    SonstigeThe residue is purified by chromatography on silica gel

Vorschrift

A mixture of N-cyclopropyl-2-(2,5-dichloropyrimidin-4-yl)-1-(ethoxymethyl)-1H-indole-4-carboxamide (30 g, 75 mmol), (1R,2R)-2-aminocyclopentanol hydrochloride (12.3 g, 90 mmol) and DIPEA (37.5 mL, 225 mmol) in DMSO (150 mL) is stirred at 80° C. for 16 h, then poured into water (1 L), and extracted with EA (2×500 mL). The combined extracts are washed with aqueous saturated sodium chloride (500 mL), dried over Na2SO4 and concentrated in vacuo. The residue is purified by chromatography on silica gel to give 2-{5-chloro-2-[(1R,2R)-2-hydroxycyclopentylamino]pyrimidin-4-yl}-N-cyclopropyl-1-(ethoxymethyl)-1H-indole-4-carboxamide (33 g, 93%). MS (m/z): 470 (35Cl) and 472 (37Cl) (M+H)+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08501166B2uspto-grants-2013_08