ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Pyridine → HCID 178487950、化合物

HRID 245724
ノート
印刷プレビュー

反応式

HRID 245724 の反応式
[OH:1][C@H:2]1[CH2:7][CH2:6][C@H:5]([C:8]2[N:12]3[CH:13]=[CH:14][N:15]=[C:16]([CH3:17])[C:11]3=[C:10]([C:18]3[CH:23]=[CH:22][C:21]([NH:24][C:25]([C:27]4[N:28]([CH3:38])[C:29]5[C:34]([CH:35]=4)=[C:33]([O:36][CH3:37])[CH:32]=[CH:31][CH:30]=5)=[O:26])=[C:20]([O:39][CH3:40])[CH:19]=3)[N:9]=2)[CH2:4][CH2:3]1.[CH:41]1([N:46]=[C:47]=[O:48])[CH2:45][CH2:44][CH2:43][CH2:42]1.N1C=CC=CC=1>CN(C)C1C=CN=CC=1.ClCCl.C(OCC)(=O)C>[CH:41]1([NH:46][C:47](=[O:48])[O:1][C@H:2]2[CH2:7][CH2:6][C@H:5]([C:8]3[N:12]4[CH:13]=[CH:14][N:15]=[C:16]([CH3:17])[C:11]4=[C:10]([C:18]4[CH:23]=[CH:22][C:21]([NH:24][C:25]([C:27]5[N:28]([CH3:38])[C:29]6[C:34]([CH:35]=5)=[C:33]([O:36][CH3:37])[CH:32]=[CH:31][CH:30]=6)=[O:26])=[C:20]([O:39][CH3:40])[CH:19]=4)[N:9]=3)[CH2:4][CH2:3]2)[CH2:45][CH2:44][CH2:43][CH2:42]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 1049PyridineHCID 643500Cyclopentyl IsocyanateHCID 178487948HCID 178487948、化合物

生成物 1

HCID 178487950HCID 178487950、化合物収率 24.9%

試薬・触媒・溶媒 3

HCID 142844-(Dimethylamino)pyridine触媒HCID 6344Dichloromethane
溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

To N-(4-(3-((trans)-4-hydroxycyclohexyl)-8-methylimidazo[1,5-a]pyrazin-1-yl)-2-methoxyphenyl)-4-methoxy-1-methyl-1H-indole-2-carboxamide (0.037 mmol, 20 mg) and N,N-dimethylpyridin-4-amine (7.41 μmol, 0.906 mg) in dichloromethane (2 ml) was added cyclopentyl isocyanate (0.185 mmol, 20.60 mg) and the mixture was stirred at room temperature overnight. Then pyridine (2 ml) was added and the mixture was stirred overnight at 90° C. The reaction mixture was diluted with ethyl acetate and the obtained suspension was filtered. The filtrate was purified by column chromatography (silica gel; dichloromethane with gradient 0 to 5% methanol) to give (trans)-4-(1-(3-methoxy-4-(4-methoxy-1-methyl-1H-indole-2-carboxamido)phenyl)-8-methylimidazo[1,5-a]pyrazin-3-yl)cyclohexyl cyclopentylcarbamate (6 mg).

後処理

  1. stirringthe mixture was stirred overnight at 90° C
  2. filtrationthe obtained suspension was filtered
  3. customThe filtrate was purified by column chromatography (silica gel; dichloromethane with gradient 0 to 5% methanol)

出典と根拠

ORDレコード
ord-85fd7182d3cd428a94b8cef7f58f9fed
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08658794B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート