Reaktion #61522

ord-772a0e79d491429d936dd965d3cf8e88

Reaktionsgleichung

COC(=O)c1cc(C(=O)O)n(Cc2cc(-c3ccc(Cl)s3)on2)n1
1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-1H-pyrazole-3,5-dicarboxylic acid 3-methyl ester
O=C1OCCN1P(=O)(Cl)N1CCOC1=O
BOP-Cl
CC(C)N1CCC(N)CC1.Cl
1-Isopropyl-piperidin-4-ylamine hydrochloride
COC(=O)c1cc(C(=O)NC2CCN(C(C)C)CC2)n(Cc2cc(-c3ccc(Cl)s3)on2)n1
1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-(1-isopropyl-piperidin-4-ylcarbamoyl)-1H-pyrazole-3-carboxylic acid methyl ester

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGwas stirred for 16 h
  2. 2
    SonstigeAfter removal of the solvent under reduced pressure the residue
  3. 3
    Sonstigewas purified by silica gel chromatography
  4. 4
    Wascheneluting with DCM/MeOH/AcOH/H2O 20:10:1:1
  5. 5
    Sonstigeto yield a white solid

Vorschrift

To 1 g 1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-1H-pyrazole-3,5-dicarboxylic acid 3-methyl ester in 10 ml DCM and 1.4 ml NEt3, 667 mg BOP-Cl were added at RT and the mixture was stirred for 30 min. After addition of 563 mg 1-Isopropyl-piperidin-4-ylamine hydrochloride the mixture was stirred for 16 h. After removal of the solvent under reduced pressure the residue was purified by silica gel chromatography eluting with DCM/MeOH/AcOH/H2O 20:10:1:1 to yield a white solid. Yield: 800 mg MS (ES+): m/e=492, chloro pattern.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07429581B2uspto-grants-2008_09