تفاعل #430276

ord-847e1346b1a045e09067198c744e4e6e

معادلة التفاعل

Cl
HCl
BrCc1ccccc1
benzyl bromide
O=C(O)c1n[nH]c2ccccc12
1H-Indazole-3-carboxylic acid
O=C([O-])[O-].[K+].[K+]
K2CO3
O=C(OCc1ccccc1)c1nn(Cc2ccccc2)c2ccccc12
title compound
O=C(OCc1ccccc1)c1nn(Cc2ccccc2)c2ccccc12
1-Benzyl-1H-indazole-3-carboxylic acid benzyl ester

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthen heated at 60° C. for 16 h
  2. 2
    درجة الحرارةThe reaction is cooled to RT
  3. 3
    استخلاصextracted with EtOAc (2×100 mL)
  4. 4
    غسيلThe organic layers are washed with H2O (2×100 mL)
  5. 5
    تجفيفdried (MgSO4)
  6. 6
    أخرىthe solvent removed in vacuo
  7. 7
    أخرىPurification of the crude material by silica gel flash column chromatography
  8. 8
    غسيلa gradient elution of hexane/EtOAc 20/1 to 2/1

الإجراء التجريبي

To a stirring solution of 750 mg (4.62 mmol) of 1H-Indazole-3-carboxylic acid (Snyder, H. R.; Thompson, C. B.; Hinman, R. L. J. Am. Chem. Soc. 1952, 74, 2009) in 20 mL of DMF is added 1.92 g (13.86 mmol, 3.0 equiv) of K2CO3, followed by 1.43 mL of benzyl bromide. The reaction mixture is stirred 15 min at RT then heated at 60° C. for 16 h. The reaction is cooled to RT, poured into 100 mL 1N HCl, and extracted with EtOAc (2×100 mL). The organic layers are washed with H2O (2×100 mL), dried (MgSO4), and the solvent removed in vacuo. Purification of the crude material by silica gel flash column chromatography using a gradient elution of hexane/EtOAc 20/1 to 2/1 afforded 735 mg of the title compound as a yellow oil which later solidified: 1H NMR (CDCl3, 300 MHz) δ8.20 (d, 1H), 7.55 (d, 2H), 7.40-7.18 (m, 11H), 5.70 (s, 2H), 5.57 (s, 2H); Rf =0.15 in hexane/EtOAc 10/1.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05859007uspto-grants-1999_01