Diisopropylethylamine → HCID 178516733、化合物

HRID 1525490ノート

反応式

HRID 1525490 の反応式
Br[C:2]1[N:3]=[C:4]2[N:11]([CH:12]3[CH2:17][CH2:16][O:15][CH2:14][CH2:13]3)[CH2:10][C:9](=[O:18])[NH:8][C:5]2=[N:6][CH:7]=1.Br[C:20]1[C:21]([NH:27][C:28](=O)CI)=[N:22][CH:23]=[C:24](Br)[N:25]=1.[CH:32](N(C(C)C)CC)(C)[CH3:33].O1CCC([NH2:47])CC1>C(#N)C>[NH:47]1[CH:28]=[N:27][C:21]([C:20]2[N:25]=[CH:24][C:23]([C:2]3[N:3]=[C:4]4[N:11]([CH:12]5[CH2:17][CH2:16][O:15][CH2:14][CH2:13]5)[CH2:10][C:9](=[O:18])[NH:8][C:5]4=[N:6][CH:7]=3)=[CH:33][CH:32]=2)=[N:22]1

参加物

6

実験手順

6-Bromo-4-(tetrahydro-2H-pyran-4-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one. To a solution of N-(3,5-dibromopyrazin-2-yl)-2-iodoacetamide (See Example 5.B) (6.6 g, 15.8 mmol) and diisopropylethylamine (4.0 g, 31.6 mmol) in acetonitrile (50 mL) was added tetrahydro-2H-pyran-4-amine (6.4 g, 63.2 mmol) and the mixture was stirred at ambient temperature for 16 h. The solvent was removed under reduced pressure and the residue which was purified by chromatography on silica gel (5-20% ethyl acetate in petroleum ether) to give the title compound (1.98 g, 40% yield). MS (ESI) m/z 313.1 [M+1]+.

後処理

  1. customThe solvent was removed under reduced pressure
  2. customthe residue which was purified by chromatography on silica gel (5-20% ethyl acetate in petroleum ether)

出典と根拠

ORDレコード
ord-ddfb5fc8c6924581922cafa69dad061e
出典データセット
uspto-grants-2015_07
特許番号
US09079900B2

反応ノート

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