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

Tributylamine → N-[4-(4-fluorophenyl)-2,2-dimethyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl]-N-(methylsulfonyl)methanesulfonamide

HRID 1479790
ノート
印刷プレビュー

反応式

HRID 1479790 の反応式
[CH3:1][C:2]1([CH3:22])[C:7](=[O:8])[NH:6][C:5]2[CH:9]=[CH:10][C:11]([N:13]([S:18]([CH3:21])(=[O:20])=[O:19])[S:14]([CH3:17])(=[O:16])=[O:15])=[CH:12][C:4]=2[O:3]1.[F:23][C:24]1[CH:29]=[CH:28][C:27](B(O)O)=[CH:26][CH:25]=1.C(N(CCCC)CCCC)CCC>CN(C)C1C=CN=CC=1.O.C([O-])(=O)C.[Cu+2].C([O-])(=O)C.CS(C)=O>[F:23][C:24]1[CH:29]=[CH:28][C:27]([N:6]2[C:5]3[CH:9]=[CH:10][C:11]([N:13]([S:18]([CH3:21])(=[O:19])=[O:20])[S:14]([CH3:17])(=[O:16])=[O:15])=[CH:12][C:4]=3[O:3][C:2]([CH3:22])([CH3:1])[C:7]2=[O:8])=[CH:26][CH:25]=1
参加物反応条件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 7622TributylamineHCID 2856454-Fluorophenylboronic acidHCID 73297136N-(2,2-dimethyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl)-N-(methylsulfonyl)methanesulfonamide

生成物 1

HCID 73294711N-[4-(4-fluorophenyl)-2,2-dimethyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl]-N-(methylsulfonyl)methanesulfonamide収率 95.4%

試薬・触媒・溶媒 3

HCID 14284
4-(Dimethylamino)pyridine
触媒
HCID 165397Cupric acetate monohydrate触媒
HCID 679Dimethyl Sulfoxide溶媒2 回

反応条件

温度
20 °C

実験手順

N-(2,2-dimethyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl)-N-(methylsulfonyl)methanesulfonamide (7.50 g), 4-fluorophenylboronic acid (5.27 g), 4-dimethylaminopyridine (0.53 g), tributylamine (3.20 g) and copper(II) acetate monohydrate (0.43 g) were added to dimethylsulfoxide (56 mL), and the mixture was stirred at 20° C. for 26 hours under blowing air (7 to 10 mL/min) thereto. The reaction mixture was added dropwise to a mixed solution of dimethylsulfoxide/concentrated hydrochloric acid/water (19 mL/4.5 g/34 mL) at about 15° C., and washed with dimethylsulfoxide (7.5 mL). The mixture was stirred at 10° C. for 3 hours, then the precipitated crystals were successively washed with dimethylsulfoxide/water (12 mL/3 mL) and water (75 mL), and then dried to obtain the title compound (9.09 g) as white crystals (yield: 95%, purity: 92%).

後処理

  1. washwashed with dimethylsulfoxide (7.5 mL)
  2. stirringThe mixture was stirred at 10° C. for 3 hours
  3. washthe precipitated crystals were successively washed with dimethylsulfoxide/water (12 mL/3 mL) and water (75 mL)
  4. customdried

出典と根拠

ORDレコード
ord-635a53138b8046cba79a9b445d7e86bb
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09409874B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート