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

Dichloromethane → HCID 178462962、化合物

HRID 717166
ノート
印刷プレビュー

反応式

HRID 717166 の反応式
Br[C:2]1[C:3]([CH3:19])=[N:4][C:5]([C:8]2[N:12]=[CH:11][N:10](C3CCCCO3)[N:9]=2)=[CH:6][CH:7]=1.B1(B2OC(C)(C)C(C)(C)O2)OC(C)(C)C(C)(C)O1.C([O-])(=O)C.[K+].C(=O)([O-])[O-].[K+].[K+].ClCCl.Br[C:53]1[N:58]=[C:57]2[N:59]([CH2:64][CH3:65])[C:60](=[O:63])[CH2:61][NH:62][C:56]2=[N:55][CH:54]=1>O1CCOCC1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].O>[CH2:64]([N:59]1[C:57]2=[N:58][C:53]([C:2]3[C:3]([CH3:19])=[N:4][C:5]([C:8]4[NH:12][CH:11]=[N:10][N:9]=4)=[CH:6][CH:7]=3)=[CH:54][N:55]=[C:56]2[NH:62][CH2:61][C:60]1=[O:63])[CH3:65]
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

10

反応物 6

HCID 6344Dichloromethane2 回HCID 11430Potassium CarbonateHCID 517044Potassium AcetateHCID 2733548Bis(pinacolato)diboraneHCID 582983093-bromo-2-methyl-6-(1-(tetrahydro-2H-pyran-2-yl)-1H-1,2,4-triazol-3-yl)pyridineHCID 866542757-bromo-1-ethyl-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one

生成物 1

HCID 178462962HCID 178462962、化合物収率 57%

試薬・触媒・溶媒 3

HCID 44119782Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)触媒2 回HCID 962Water溶媒HCID 312751,4-Dioxane溶媒

反応条件

温度
90 °C

実験手順

A mixture of 3-Bromo-2-methyl-6-(1-(tetrahydro-2H-pyran-2-yl)-1H-1,2,4-triazol-3-yl)pyridine (1 equiv), bis(pinacolato)diboron (1.05 equiv), potassium acetate (2 equiv), potassium carbonate (3 equiv), [1,1′-bis(diphenylphosphino)-ferrocene]dichloropalladium(II), complex with dichloromethane (1:1) (0.1 equiv) in anhydrous dioxane was degassed and heated at 90° C. for 2 h. The mixture was cooled to <40° C. and 7-bromo-1-ethyl-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one (1 equiv), water and [1,1′-bis(diphenylphosphino)-ferrocene]dichloropalladium(II), complex with dichloromethane (1:1) (0.05 equiv) were added. The mixture was degassed and heated at 65-70° C. under nitrogen for 1 h. The mixture was cooled to <40° C., diluted with water and ethyl acetate. Standard ethyl acetate/water work up followed by flash column chromatography (0-5% methanol in dichloromethane) gave the title compound in 57% yield. 1H NMR (400 MHz, DMSO-d6) δ (ppm) 7.99 (s, 2H), 7.93 (s, 1H), 7.72 (s, 1H), 4.22 (s, 2H), 4.05 (q, J=6.77 Hz, 2H), 2.71 (s, 3H), 1.18 (t, J=7.03 Hz, 3H); MS (ESI) m/z 337.6 [M+1]+.

後処理

  1. customwas degassed
  2. temperatureThe mixture was cooled to <40° C.
  3. customThe mixture was degassed
  4. temperatureheated at 65-70° C. under nitrogen for 1 h
  5. temperatureThe mixture was cooled to <40° C.
  6. additiondiluted with water and ethyl acetate

出典と根拠

ORDレコード
ord-2070d6a96d94444082be9758fdfc805f
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09193692B2

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