Réaction #1973922

ord-1c27028976634010ba50d1885c017ffc

Équation de réaction

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
Rendement 93.6%

Solvants

Conditions de réaction

Température
80°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionextracted with EA (2×500 mL)
  2. 2
    LavageThe combined extracts are washed with aqueous saturated sodium chloride (500 mL)
  3. 3
    Séchagedried over Na2SO4
  4. 4
    Concentrationconcentrated in vacuo
  5. 5
    AutreThe residue is purified by chromatography on silica gel

Mode opératoire

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)+.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08501166B2uspto-grants-2013_08