3-Iodopyridine → HCID 16739631、化合物

HRID 19879

反応式

HRID 19879 の反応式
[F:1][C:2]1([F:29])[CH2:7][CH2:6][N:5]([C:8]([C:10]2[NH:11][C:12]3[C:17]([CH:18]=2)=[CH:16][C:15]([O:19][CH:20]2[CH2:25][CH2:24][N:23]([CH:26]([CH3:28])[CH3:27])[CH2:22][CH2:21]2)=[CH:14][CH:13]=3)=[O:9])[CH2:4][CH2:3]1.I[C:31]1[CH:32]=[N:33][CH:34]=[CH:35][CH:36]=1>>[F:29][C:2]1([F:1])[CH2:7][CH2:6][N:5]([C:8]([C:10]2[N:11]([C:31]3[CH:32]=[N:33][CH:34]=[CH:35][CH:36]=3)[C:12]3[C:17]([CH:18]=2)=[CH:16][C:15]([O:19][CH:20]2[CH2:25][CH2:24][N:23]([CH:26]([CH3:27])[CH3:28])[CH2:22][CH2:21]2)=[CH:14][CH:13]=3)=[O:9])[CH2:4][CH2:3]1

参加物

3

反応物 2

HCID 707143-IodopyridineHCID 11603838(4,4-Difluoropiperidin-1-yl)[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]methanone2 回

生成物 1

HCID 16739631HCID 16739631、化合物

実験手順

In analogy to the procedure described for the synthesis of example 34, the title compound was synthesized from (4,4-difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone (intermediate 1) and 3-iodopyridine. The title compound was obtained in 82% yield as light brown foam. MS (m/e): 483.3 (MH+, 100%).

後処理

  1. customIn analogy to the procedure described for the synthesis of example 34

出典と根拠

ORDレコード
ord-575654b870f049e8b4293f9883d851fd
出典データセット
uspto-grants-2010_06
特許番号
US07745479B2

関連ノート

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