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

Dimethylformamide → ethyl (4S)-6-cyano-2-ethyl-8-methoxy-4-methyl-1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-7-carboxylate

HRID 494136
ノート
印刷プレビュー

反応式

HRID 494136 の反応式
Br[C:2]1[N:6]2[C@@H:7]([CH3:14])[CH2:8][N:9]([CH2:12][CH3:13])[C:10](=[O:11])[C:5]2=[C:4]([O:15][CH3:16])[C:3]=1[C:17]([O:19][CH2:20][CH3:21])=[O:18].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH3:41][N:42](C=O)C>[Zn].[C-]#N.[Zn+2].[C-]#N.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[C:41]([C:2]1[N:6]2[C@@H:7]([CH3:14])[CH2:8][N:9]([CH2:12][CH3:13])[C:10](=[O:11])[C:5]2=[C:4]([O:15][CH3:16])[C:3]=1[C:17]([O:19][CH2:20][CH3:21])=[O:18])#[N:42]
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 6228DimethylformamideHCID 11776TriphenylphosphineHCID 86624798(S)-Ethyl 6-bromo-2-ethyl-8-methoxy-4-methyl-1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-7-carboxylate

生成物 1

HCID 86624801ethyl (4S)-6-cyano-2-ethyl-8-methoxy-4-methyl-1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-7-carboxylate

試薬・触媒・溶媒 3

HCID 11186Zinc cyanide (Zn(CN)2)
触媒
HCID 23994Zinc触媒
HCID 9811564Bis(dibenzylideneacetone)palladium触媒

反応条件

温度
140 °C

実験手順

To a mixture of ethyl (4S)-6-bromo-2-ethyl-8-methoxy-4-methyl-1-oxo-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-7-carboxylate (4.1 g, 11.41 mmol; Example 62, step 7), zinc dust (0.15 g, 2.28 mmol), zinc cyanide (1.11 g, 9.47 mmol), triphenylphosphine (0.46 g, 1.77 mmol), and tris(dibenzylideneacetone)dipalladium (0) (1.57 g, 1.71 mmol) in anhydrous DMF (10 mL) was purged with argon gas for 15 minutes. The mixture was heated in a sealed tube in an oil bath at 140° C. overnight. The reaction mixture was filtered through a pad of Celite, and the filtrate concentrated under vacuum. The residue was partitioned between chloroform and aqueous EDTA monosodium salt. The mixture was stirred at room temperature for 30 minutes. The organic extract was washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum. The residue was subjected to column chromatography on silica gel eluted with 0 to 40% ethyl acetate in chloroform gradient. Collection and concentration of appropriate fractions provided the title nitrile.

後処理

  1. customwas purged with argon gas for 15 minutes
  2. filtrationThe reaction mixture was filtered through a pad of Celite
  3. concentrationthe filtrate concentrated under vacuum
  4. customThe residue was partitioned between chloroform and aqueous EDTA monosodium salt
  5. extractionThe organic extract
  6. washwas washed with brine
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated under vacuum
  10. washeluted with 0 to 40% ethyl acetate in chloroform gradient
  11. customCollection and concentration of appropriate fractions

出典と根拠

ORDレコード
ord-18708559f83344628014bb586263e8d6
出典データセット
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07538112B2

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