Reaktion #61068

ord-2154f7a9e0494f7ca847e5d03c3df2d0

Reaktionsgleichung

O
water
O=C(Cl)CCCCl
4-Chloro-butyryl chloride
Nc1cc[nH]n1
3-aminopyrazole
O=P([O-])([O-])O.[K+].[K+]
K2HPO4
O=C(CCCCl)Nc1ccn(C(=O)CCCCl)n1
title compound
Ausbeute 34.0%
O=C(CCCCl)Nc1ccn(C(=O)CCCCl)n1
4-Chloro-N-[1-(4-chlorobutanoyl)-1H-pyrazol-3-yl]butanamide
Ausbeute 34.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGthe reaction mixture was stirred for 24 hr
  2. 2
    Sonstigethe phases were separated
  3. 3
    ExtraktionThe aqueous layer was extracted with EtOAc (2×20 mL)
  4. 4
    Trocknenthe combined organic extracts were dried over anh. Na2SO4
  5. 5
    FiltrationThe solids were filtered
  6. 6
    Sonstigethe solvent evaporated
  7. 7
    SonstigeThe crude product was purified by flash chromatography (silica gel, cHex/EtOAc 7:3)

Vorschrift

To a solution of 3-aminopyrazole (300 mg, 3.61 mmol) in anh. CH2Cl2 (6 mL), at r.t., under N2, was added K2HPO4 (1.26 g, 2 eq) and the reaction mixture was stirred at r.t. for 15 min. 4-Chloro-butyryl chloride (406 μL, 3.6 mmol) was then added and the reaction mixture was stirred for 24 hr. It was then poured into water and the phases were separated. The aqueous layer was extracted with EtOAc (2×20 mL) and the combined organic extracts were dried over anh. Na2SO4. The solids were filtered and the solvent evaporated. The crude product was purified by flash chromatography (silica gel, cHex/EtOAc 7:3) to give the title compound as a white solid (354 mg, 34%)

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07427630B2uspto-grants-2008_09