تفاعل #8192

ord-30b6def8a1514691b9d38b1893394da3

معادلة التفاعل

CC(C)(Cc1c[nH]c2c(O)cccc12)NC(=O)OC(C)(C)C
[2-(7-hydroxy-1H-indol-3-yl)-1,1-dimethyl-ethyl]-carbamic acid tert-butyl ester
N#CCBr
bromoacetonitrile
O=C([O-])[O-].[K+].[K+]
K2CO3
CC(C)(Cc1c[nH]c2c(OCC#N)cccc12)NC(=O)OC(C)(C)C
[2-(7-cyanomethoxy-1H-indol-3-yl)-1,1-dimethyl-ethyl]-carbamic acid tert-butyl ester
المردود 86.5%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةis heated to reflux
  2. 2
    درجة الحرارةto cool
  3. 3
    ترشيحis filtered through celite
  4. 4
    تركيزThe filtrate is concentrated to an oil which
  5. 5
    أخرىis purified by flash chromatography with CH2Cl2

الإجراء التجريبي

A mixture of [2-(7-hydroxy-1H-indol-3-yl)-1,1-dimethyl-ethyl]-carbamic acid tert-butyl ester (15.55 g, 51.1 mmol), bromoacetonitrile (10.7 mL, 153 mmol), K2CO3 (17.78 g, 128.6 mmol) and 2-butanone is heated to reflux. After 1 hour the mixture is allowed to cool and is filtered through celite. The filtrate is concentrated to an oil which is purified by flash chromatography with CH2Cl2 followed by 5% ethyl acetate/CH2Cl2 to give 15.18 g of [2-(7-cyanomethoxy-1H-indol-3-yl)-1,1-dimethyl-ethyl]-carbamic acid tert-butyl ester (86%). MS (ES−) m/z 342.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07087635B2uspto-grants-2006_08