تفاعل #1483067

ord-46a8c47f49664915a044db974d078b71

معادلة التفاعل

COC(=O)c1ccc2cc[nH]c2c1
1H-indole-6-carboxylic acid methyl ester
FC(F)Oc1ccc(CBr)cc1
4-difluoromethoxy-benzyl bromide
[H-].[Na+]
sodium hydride
COC(=O)c1ccc2ccn(Cc3ccc(OC(F)F)cc3)c2c1
1-(4-difluoromethoxy-phenylmethyl)-1H-indole-6-carboxylic acid methyl ester
المردود 21.1%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلthe organic layer was washed again with dilute NaHCO3 (25 mL)
  2. 2
    تجفيفThe organic layer was dried over Na2SO4
  3. 3
    ترشيحfiltered
  4. 4
    تركيزconcentrated

الإجراء التجريبي

To a solution of commercially available 1H-indole-6-carboxylic acid methyl ester (0.35 g, 2.0 mmol) and 4-difluoromethoxy-benzyl bromide (0.52 g, 2.2 mmol) in DMF (2 mL) was added sodium hydride (92 mg, 2.3 mmol). After stirring at room temperature for 3.5 hr, the solution was diluted with water (25 mL) and ethyl acetate (75 mL), the organic layer was washed again with dilute NaHCO3 (25 mL) and then brine (25 mL). The organic layer was dried over Na2SO4, filtered and concentrated. The remaining residue was subjected to flash chromatography (ethyl acetate/hexane. 1:5) to provide 1-(4-difluoromethoxy-phenylmethyl)-1H-indole-6-carboxylic acid methyl ester as a colorless oil (0.14 g, 21% yield).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08900565B2uspto-grants-2014_12