Diisopropylethylamine → 4-[5-(3-Chloro-5-fluoro-phenyl)-1-(3-pyridyl)pyrazole-3-carbonyl]piperazin-2-one

HRID 930048ノート

反応式

HRID 930048 の反応式
C(N(CC)C(C)C)(C)C.[Cl:10][C:11]1[CH:12]=[C:13]([C:18]2[N:22]([C:23]3[CH:24]=[N:25][CH:26]=[CH:27][CH:28]=3)[N:21]=[C:20]([C:29]([OH:31])=O)[CH:19]=2)[CH:14]=[C:15]([F:17])[CH:16]=1.[O:32]=[C:33]1[CH2:38][NH:37][CH2:36][CH2:35][NH:34]1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F>C1COCC1>[Cl:10][C:11]1[CH:12]=[C:13]([C:18]2[N:22]([C:23]3[CH:24]=[N:25][CH:26]=[CH:27][CH:28]=3)[N:21]=[C:20]([C:29]([N:37]3[CH2:36][CH2:35][NH:34][C:33](=[O:32])[CH2:38]3)=[O:31])[CH:19]=2)[CH:14]=[C:15]([F:17])[CH:16]=1

参加物

6

実験手順

0.07 ml (0.43 mmol) of N,N-diisopropylethylamine is added to a solution of 75 mg (0.21 mmol, 90% purity) of the compound of Example 22A, 23 mg (0.23 mmol) of 2-oxopiperazine, and 113 mg (0.30 mmol) of HATU in 2 ml of THF, and the mixture that is obtained is stirred for 3 hours at room temperature. The reaction mixture is separated by means of preparative HPLC (mobile solvent: acetonitrile/water gradient), and the title compound is obtained in a quantitative yield (87 mg).

後処理

  1. customthe mixture that is obtained
  2. customThe reaction mixture is separated by means of preparative HPLC (mobile solvent: acetonitrile/water gradient)

出典と根拠

ORDレコード
ord-18e289a9e3ac419889cece7242c2fdaa
出典データセット
uspto-grants-2016_03
特許番号
US09296720B2

反応ノート

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