Реакция #10017

ord-070783df20e7489689e0498417256699

Уравнение реакции

CCn1cnc2c(Nc3ccc(N)cc3)nc(NCCO)nc21
6-(4-amino-phenyl-amino)-9-ethyl-2-(2-hydroxy-ethyl-amino)-9H-purine
CN(C)[P+](On1nnc2ccccc21)(N(C)C)N(C)C.F[P-](F)(F)(F)(F)F
(benzotriazol-1-yloxy)-tris-(dimethylamino)-phosphonium hexafluorophosphate
On1nnc2ccccc21
1-hydroxybenzotriazole
CC(C)NC(C)C
diisopropylamine
O=C(O)c1cccc(Cl)c1
3-chlorobenzoic acid
CCn1cnc2c(Nc3ccc(NC(=O)c4cccc(Cl)c4)cc3)nc(NCCO)nc21
6-(4-[3-Chloro-benzoyl-amino]-phenyl-amino)-9-ethyl-2-(2-hydroxy-ethyl-amino)-9H-purine

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Промывкаwashed with water
  2. 2
    ДругоеThe crude product is purified by chromatography over silica gel (mobile phase: methylene chloride:methanol=9:1)

Методика

62 mg (0.2 mmol) of 6-(4-amino-phenyl-amino)-9-ethyl-2-(2-hydroxy-ethyl-amino)-9H-purine (prepared according to Example 108), 0.18 g (0.4 mmol) of (benzotriazol-1-yloxy)-tris-(dimethylamino)-phosphonium hexafluorophosphate (BOP), 54 mg (0.4 mmol) of 1-hydroxybenzotriazole (HOBT) and 68 μl of diisopropylamine are stirred in 6 ml of dimethylacetamide at RT for 5 min and then treated with 63 mg (0.4 mmol) of 3-chlorobenzoic acid. After the reaction mixture has been stirred at RT for 30 min, it is diluted with ethyl acetate and washed with water. The crude product is purified by chromatography over silica gel (mobile phase: methylene chloride:methanol=9:1). 6-(4-[3-Chloro-benzoyl-amino]-phenyl-amino)-9-ethyl-2-(2-hydroxy-ethyl-amino)-9H-purine is obtained; FAB-MS: (M+H)+=452; Rf=0.45 (methylene chloride:methanol=9:1).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07091346B1uspto-grants-2006_08