Reaction #1973921

ord-e97d1b8244cc471283379ac0d6e4ff7d

Reaction equation

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
(1S,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,2S)-2-hydroxycyclopentylamino]pyrimidin-4-yl}-N-cyclopropyl-1-(ethoxymethyl)-1H-indole-4-carboxamide
Yield 60.3%

Solvents

Conditions

Temperature
100°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Extractionextracted with EA
  2. 2
    WashThe combined extracts are washed with aqueous saturated sodium chloride
  3. 3
    Dryingdried over Na2SO4
  4. 4
    Concentrationconcentrated in vacuo
  5. 5
    OtherThe residue is purified by chromatography on silica gel

Procedure

A mixture of N-cyclopropyl-2-(2,5-dichloropyrimidin-4-yl)-1-(ethoxymethyl)-1H-indole-4-carboxamide (10 g, 25 mmol), (1S,2R)-2-aminocyclopentanol hydrochloride (4.1 g, 30 mmol) and DIPEA (5 mL, 30 mmol) in DMSO (70 mL) is stirred at 100° C. for 3 h, then poured into water and extracted with EA. The combined extracts are washed with aqueous saturated sodium chloride, dried over Na2SO4 and concentrated in vacuo. The residue is purified by chromatography on silica gel to give 2-{5-chloro-2-[(1R,2S)-2-hydroxycyclopentylamino]pyrimidin-4-yl}-N-cyclopropyl-1-(ethoxymethyl)-1H-indole-4-carboxamide (7 g, 60.3%). MS (m/z): 470 (35Cl) and 472 (37Cl) (M+H)+

Source

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