Tetrahydrofuran → (S)-6-bromo-1-(1-phenylethyl)-1H-imidazo[4,5-b]pyrazin-2-ol

HRID 1014689ノート

反応式

HRID 1014689 の反応式
[Br:1][C:2]1[N:7]=[C:6]2[N:8]([C@H:12]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[CH3:13])[C:9](=[O:11])[NH:10][C:5]2=[N:4][CH:3]=1.BrC1N=C(N[C@H:28]([C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)[CH3:29])C(N)=NC=1.[C:37](N1C=CN=C1)([N:39]1C=CN=C1)=O.O1CCC[CH2:50]1>CO>[CH3:50][N:10]1[C:5]2=[N:4][CH:3]=[C:2]([C:35]3[CH:34]=[CH:33][CH:32]=[C:31]4[C:30]=3[CH:28]=[CH:29][CH:37]=[N:39]4)[N:7]=[C:6]2[N:8]([C@H:12]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH3:13])[C:9]1=[O:11].[Br:1][C:2]1[N:7]=[C:6]2[N:8]([C@H:12]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[CH3:13])[C:9](=[O:11])[NH:10][C:5]2=[N:4][CH:3]=1

参加物

7

実験手順

(S)-6-Bromo-1-(1-phenylethyl)-1H-imidazo[4,5-b]pyrazin-2(3H)-one. The title compound was prepared using (S)-6-bromo-N2-(1-phenylethyl)pyrazine-2,3-diamine (See Example 3.A) (0.50 g, 1.71 mmol), 1,1′-carbonyldiimidazole (0.35 g, 2.13 mmol), and tetrahydrofuran (7 mL) as described in General Procedure D1. The crude material was dissolved in methanol (5 mL), and the product was triturated with H2O while sonicating. The resulting precipitate was filtered and dried in a vacuum oven overnight to afford 0.34 g (1.07 mmol, 62%) of (S)-6-bromo-1-(1-phenylethyl)-1H-imidazo[4,5-b]pyrazin-2(3H)-one. MS (ESI) m/z 319.4 [M+1]+.

後処理

  1. customthe product was triturated with H2O
  2. customwhile sonicating
  3. filtrationThe resulting precipitate was filtered
  4. customdried in a vacuum oven overnight

出典と根拠

ORDレコード
ord-1cf93a1c93c04bed9b2e2c516efd9e45
出典データセット
uspto-grants-2011_07
特許番号
US07981893B2

反応ノート

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