Reaktion #722830

ord-024d5be90d9c4a2eb11be3eb3f2cfa2b

Reaktionsgleichung

Cc1nc(Cl)c2nc(-c3ccccc3)cc-2[nH]1
4-chloro-2-methyl-6-phenylpyrrolo[3,2-d]pyrimidine
CCCCC(CC)CN
2-ethylhexylamine
O=C([O-])[O-].[K+].[K+]
K2CO3
CCCCC(CC)CNc1nc(C)[nH]c2cc(-c3ccccc3)nc1-2
title compound
Ausbeute 63.0%
CCCCC(CC)CNc1nc(C)[nH]c2cc(-c3ccccc3)nc1-2
(2-Ethylhexyl)(2-methyl-6-phenylpyrrolo[2,3-e]pyrimidin-4-yl)amine
Ausbeute 63.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThis compound was prepared

Vorschrift

This compound was prepared according to the method described in Example 2 by employing 4-chloro-2-methyl-6-phenylpyrrolo[3,2-d]pyrimidine (Example 1(e)) (70.0 mg, 0.29 mmol), 2-ethylhexylamine (Aldrich Chemical Company) (0.24 mL, 1.44 mmol) and K2CO3 (0.40 g, 2.87 mmol) in H2O (2 mL) to give 61 mg (63%) of the title compound as a white solid. An analytical sample was obtained by recrystallization from i-PrOH. Mp: 288-289° C. (dec.). 1H NMR (CDCl3; 500 MHz): δ 0.72-0.78 (m, 6), 1.15-1.34 (m, 9), 2.62 (s, 3), 3.56 (dd, 2, J=5.3, 7.6), 6.71 (s, 2), 7.17-7.24 (m, 3), 7.59 (d, 2, J=7.6), 12.78 (br s, 1). MS m/z: 337 (M+1), 335 (M−1). HRMS: Calcd for M+H: 337.2392. Found: 337.2397.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06187777B1uspto-grants-2001_02