تفاعل #303356

ord-3cc7ff80c51c45c28d537c919ff3f1d4

معادلة التفاعل

Cc1nc(NCCc2ccc(Cl)cc2Cl)cc(-c2cccc(C(C)(C)C#N)c2)n1
2-(3-{6-[2-(2,4-dichloro-phenyl)-ethylamino]-2-methyl-pyrimidin-4-yl}-phenyl)-2-methyl-propionitrile
Cc1nc(NCCc2ccc(Cl)cc2Cl)cc(-c2cccc(C(C)(C)C#N)c2)n1
2-(3-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methyl-pyrimidin-4-yl}-phenyl)-2-methyl-propionitrile
Cc1nc(NCCc2ccc(Cl)cc2Cl)cc(-c2cccc(C(C)(C)C#N)c2)n1
Intermediate ( 67 )
Cc1nc(NCCc2ccc(Cl)cc2Cl)cc(-c2cccc(C(C)(C)C#N)c2)n1
2-(3-{6-[2-(2,4-Dichloro-phenyl)-ethylamino]-2-methyl-pyrimidin-4-yl}-phenyl)-2-methyl-propionitrile
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[N]=[N+]=[N-]
azidotributyltin
Cc1nc(NCCc2ccc(Cl)cc2Cl)cc(-c2cccc(C(C)(C)c3nn[nH]n3)c2)n1
[2-(2,4-dichloro-phenyl)-ethyl]-(2-methyl-6-{3-[1-methyl-1-(2H-tetrazol-5-yl)-ethyl]-phenyl}-pyrimidin-4-yl)-amine

ظروف التفاعل

درجة الحرارة
180°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىReaction mixture
  2. 2
    تركيزis concentrated
  3. 3
    أخرىpurified via silica gel chromatography
  4. 4
    غسيلeluting with 20 to 100% EtOAc in heptane

الإجراء التجريبي

To a solution of 2-(3-{6-[2-(2,4-dichloro-phenyl)-ethylamino]-2-methyl-pyrimidin-4-yl}-phenyl)-2-methyl-propionitrile [50 mg, 0.11 mmol, Intermediate (67)] in α, α, α-trifluorotoluene (2 mL) is added azidotributyltin (0.251 mL, 0.88 mmol) and heated in microwave oven at 180° C. for 1.5 hours. Reaction mixture is concentrated and purified via silica gel chromatography eluting with 20 to 100% EtOAc in heptane to give [2-(2,4-dichloro-phenyl)-ethyl]-(2-methyl-6-{3-[1-methyl-1-(2H-tetrazol-5-yl)-ethyl]-phenyl}-pyrimidin-4-yl)-amine as a solid, which is treated with 1M hydrogen chloride in ether affording [2-(2,4-dichloro-phenyl)-ethyl]-(2-methyl-6-{3-[1-methyl-1-(2H-tetrazol-5-yl)-ethyl]-phenyl}-pyrimidin-4-yl)-amine hydrochloride [47 mg, 80%, Example 47] as a solid. LC/MS: RT=2.47 minutes, MS: 484 (M+H). 1H NMR [300 MHz, (CD3)2SO]: □8.64 (1H, br s), 7.3-7.8 (7H, m), 6.56 (1H, s), 3.98 (3H, s), 3.64 (2H, m), 3 (2H, m), 1.8 (6H, s). IC50=0.4 nM

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08193183B2uspto-grants-2012_06