تفاعل #1350574

ord-afaf075ecc404ad580a3fdea35c06371

معادلة التفاعل

Cn1cc(Br)c(-c2cccc(N)c2)n1
3-(3-aminophenyl)-4-bromo-1-methylpyrazole
CCN(CC)CC
triethylamine
O=C(O)Cc1ccc(OC(F)(F)F)cc1
4-trifluoromethoxyphenylacetic acid
CN(C)C(On1nnc2ccccc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HBTU
On1nnc2ccccc21
HOBT
Cn1cc(Br)c(-c2cccc(NC(=O)Cc3ccc(OC(F)(F)F)cc3)c2)n1
title compound
المردود 68.0%
Cn1cc(Br)c(-c2cccc(NC(=O)Cc3ccc(OC(F)(F)F)cc3)c2)n1
N-[3-(4-bromo-1-methylpyrazol-3-yl)phenyl]-2-[4-(trifluoromethoxy)phenyl]acetamide
المردود 68.0%

المذيبات

ظروف التفاعل

درجة الحرارة
70°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىquenched with aqueous sodium bicarbonate solution
  2. 2
    workup.ADDITIONEthyl acetate was added
  3. 3
    أخرىthe organic phase separated
  4. 4
    غسيلwashed with water (×3), brine
  5. 5
    تجفيفdried (MgSO4)
  6. 6
    أخرىevaporated

الإجراء التجريبي

A solution of 3-(3-aminophenyl)-4-bromo-1-methylpyrazole (35 mg, 0.14 mmol) and triethylamine (23 μL, 0.17 mmol) in DMF (0.5 mL) was added in one portion to a stirred solution of 4-trifluoromethoxyphenylacetic acid (31 mg, 0.14 mmol), HBTU (53 mg, 0.14 mmol) and HOBT (19 mg, 0.14 mmol) in DMF (1 mL). The mixture was heated at 70° C. for 24 h and then quenched with aqueous sodium bicarbonate solution. Ethyl acetate was added and the organic phase separated, washed with water (×3), brine, dried (MgSO4) and evaporated. Chromatography on flash silica (50% EtOAc/hexane) gave the title compound as a colourless solid (43 mg, 68%), m.p. 141.2-142.5° C. (EtOAc/hexane).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06541209B1uspto-grants-2003_04