Imidazole → 2-Imidazol-1-yl-4-(4-methoxy-benzylamino)-thieno[3,2-c]pyridine-7-carbonitrile

HRID 1868300ノート

反応式

HRID 1868300 の反応式
[NH:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.C([O-])([O-])=O.[Cs+].[Cs+].I[C:13]1[S:21][C:20]2[C:19]([C:22]#[N:23])=[CH:18][N:17]=[C:16]([NH:24][CH2:25][C:26]3[CH:31]=[CH:30][C:29]([O:32][CH3:33])=[CH:28][CH:27]=3)[C:15]=2[CH:14]=1>[Cu]I.O1CCOCC1>[N:1]1([C:13]2[S:21][C:20]3[C:19]([C:22]#[N:23])=[CH:18][N:17]=[C:16]([NH:24][CH2:25][C:26]4[CH:31]=[CH:30][C:29]([O:32][CH3:33])=[CH:28][CH:27]=4)[C:15]=3[CH:14]=2)[CH:5]=[CH:4][N:3]=[CH:2]1

参加物

6

実験手順

To an oven dried Schlenk tube was added CuI (0.0057 g, 0.030 mmol), imidazole (0.097 g, 1.42 mmol), Cs2CO3 (0.405 g, 1.25 mmol). The tube was evacuated and purged to argon 5 times. Under argon, the tube was supplied with 2-iodo-4-(4-methoxy-benzylamino)-thieno[3,2-c]pyridine-7-carbonitrile 27 (0.25 g, 0.59 mmol) trans-1,2-cyclohexanediamine (0.014 mL, 0.12 mmol), and dioxane (1 mL). The reaction contents were briefly evacuated and the vessel purged to argon 3 times, then sealed and brought to 110° C. with stirring. After 24 h, 20 mL of CH2Cl2 were added to the cooled reaction. The mixture was filtered and solvents removed in vacuo. Silica gel column chromatography (eluent: 3% MeOH in CH2Cl2) provided 0.12 g of 37. 1H NMR (400 MHz, d6-DMSO) δ 8.57 (t, J=6 Hz, 1H), 8.47 (s, 1H), 8.23 (bs, 1H), 8.00 (s, 1H), 7.71 (bs, 1H), 7.31 (d, J=8 Hz, 2H), 7.21 (bs, 1H), 6.91 (d, J=8 Hz, 2H), 3.74 (s, 3H).

後処理

  1. customTo an oven dried Schlenk tube
  2. customThe tube was evacuated
  3. custompurged to argon 5 times
  4. customThe reaction contents
  5. customwere briefly evacuated
  6. customthe vessel purged to argon 3 times
  7. customsealed
  8. custombrought to 110° C.
  9. addition20 mL of CH2Cl2 were added to the cooled reaction
  10. filtrationThe mixture was filtered
  11. customsolvents removed in vacuo

出典と根拠

ORDレコード
ord-7a801c634ab4402b89de481fd0ef58fe
出典データセット
uspto-grants-2009_12
特許番号
US07635695B2

反応ノート

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