تفاعل #70695

ord-2ec91820c55d421f8ac725e65f16ef79

معادلة التفاعل

[Na+].[OH-]
NaOH
CC(C)n1ccc2c(Br)cc(C(F)(F)F)cc21
4-bromo-1-(1-methylethyl)-6-(trifluoromethyl)-1H-indole
N#[C][Zn][C]#N
dicyanozinc
COc1cccc(OC)c1-c1ccccc1P(C1CCCCC1)C1CCCCC1
s-Phos
CC(C)n1ccc2c(C#N)cc(C(F)(F)F)cc21
title compound
المردود 77.2%
CC(C)n1ccc2c(C#N)cc(C(F)(F)F)cc21
1-Isopropyl-6-(trifluoromethyl)-1H-indole-4-carbonitrile
المردود 77.2%

المذيبات

ظروف التفاعل

درجة الحرارة
120°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe mixture was degassed for 5 min
  2. 2
    أخرىby bubbling N2
  3. 3
    أخرىThe tube was sealed
  4. 4
    استخلاصthe mixture was extracted with EtOAc (3×)
  5. 5
    تجفيفThe extract was dried over Na2SO4
  6. 6
    تركيزconcentrated
  7. 7
    أخرىThe residue was purified

الإجراء التجريبي

To a 10-mL microwave tube were added 4-bromo-1-(1-methylethyl)-6-(trifluoromethyl)-1H-indole (330 mg, 1.078 mmol), dicyanozinc (146 mg, 1.240 mmol), DMF (4 mL) and water (0.040 mL), and the mixture was degassed for 5 min by bubbling N2. s-Phos (48.7 mg, 0.119 mmol) and tris(dibenzylideneacetone)dipalladium(0) (49.4 mg, 0.054 mmol) were added. The tube was sealed and the mixture was heated at 120° C. for 2.5 h. 1 N NaOH (3 mL) was added and the mixture was extracted with EtOAc (3×). The extract was dried over Na2SO4 and concentrated. The residue was purified using column chromatography (Silica gel, 0 to 70% EtOAc/hexanes) to give the title compound (210 mg, 77%) as white solid. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.61 (m, 6H), 4.79 (spt, J=6.69 Hz, 1H), 6.84 (d, J=3.28 Hz, 1H), 7.59 (d, J=3.28 Hz, 1H), 7.73 (s, 1H), 7.88 (s, 1H). MS: (M+H)+=253.2.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08536179B2uspto-grants-2013_09