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Dichloromethane → 7-(4-Ethyl-5-fluoropyridin-3-yl)-6-fluoro-1-methyl-4,5-dihydro-[1,2,4]-triazolo[4,3-a]quinoline

HRID 1521661
ノート
印刷プレビュー

反応式

HRID 1521661 の反応式
Br[C:2]1[C:3]([F:16])=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]1[C:12]([CH3:15])=[N:13][N:14]=[C:7]1[CH2:6][CH2:5]2.[CH2:17]([C:19]1[C:24](B2OC(C)(C)C(C)(C)O2)=[CH:23][N:22]=[CH:21][C:20]=1[F:34])[CH3:18].C(=O)([O-])[O-].[Na+].[Na+].ClCCl>O.O1CCOCC1>[CH2:17]([C:19]1[C:20]([F:34])=[CH:21][N:22]=[CH:23][C:24]=1[C:2]1[C:3]([F:16])=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]1[C:12]([CH3:15])=[N:13][N:14]=[C:7]1[CH2:6][CH2:5]2)[CH3:18]
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 4

HCID 6344DichloromethaneHCID 10340Sodium CarbonateHCID 709774807-Bromo-6-fluoro-1-methyl-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinolineHCID 709778534-Ethyl-3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

生成物 1

HCID 899618507-(4-Ethyl-5-fluoropyridin-3-yl)-6-fluoro-1-methyl-4,5-dihydro-[1,2,4]-triazolo[4,3-a]quinoline

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 312751,4-Dioxane溶媒

反応条件

温度
100 °C

実験手順

To a stirred solution of 7-bromo-6-fluoro-1-methyl-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinoline (146-7; 0.2 g, 0.00704 mol) and 4-ethyl-3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (0.21 g, 0.0084 mol) in the mixture of 1,4-dioxan (5 mL) and water (5 mL) was added sodium carbonate (0.186 g, 0.0176 mol). Reaction mass was purged with argon for the next 20 min. Catalyst Pd(dppf)2Cl2.dichloromethane (0.28 g, 0.00352 mol) was added and again purged with argon for 10 min and allowed to stir at 100° C. for 12 h. The reaction mixture was filtered through CELITE bed and filter bed was thoroughly washed with ethyl acetate. The collected organic parts was concentrated under vacuum to afford the crude compound, which was purified by silica gel column chromatography followed by preparative HPLC (analytical conditions: column: ZORBAX XDB (150 mm×4.6 mm×3.5 μm), mobile phase (A): water, mobile phase (B): methanol, flow rate: 1.0 mL/min, gradient T/% B:0/20,8/70,25/70,27/20,30/20) to obtain title compound. 1H NMR (400 MHz, CDCl3-d6) δ 8.451 (s, 1H), 8.238 (s, 1H), 7.427-7.406 (d, J=8.4 Hz, 1H), 7.297-7.278 (d, J=7.6 Hz, 1H), 3.219-3.184 (t, J=6.4 Hz, 2H), 3.132-3.097 (t, J=7.6 Hz, 2H), 2.812 (s, 3H), 2.604-2.586 (d, J=7.2 Hz, 2H), 1.130-1.093 (t, J=7.6 Hz, 3H). MS (M+1): 327.1.

後処理

  1. customReaction mass
  2. customwas purged with argon for the next 20 min
  3. customagain purged with argon for 10 min
  4. filtrationThe reaction mixture was filtered through CELITE bed
  5. filtrationfilter bed
  6. washwas thoroughly washed with ethyl acetate
  7. concentrationThe collected organic parts was concentrated under vacuum
  8. customto afford the crude compound, which
  9. customwas purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-0a847912ac064e948d6899e21159d350
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09073929B2

反応ノート

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