Lithium Chloride → 5-(4-(Hydroxymethyl)thiazol-2-yl)-1,3-dimethyl-6-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[3,4-d]pyrimidine-2,4(3H,6H)-dione

HRID 2201318ノート

反応式

HRID 2201318 の反応式
[BH4-].[Na+].[CH3:3][N:4]1[C:9]2=[CH:10][N:11]([CH2:23][O:24][CH2:25][CH2:26][Si:27]([CH3:30])([CH3:29])[CH3:28])[C:12]([C:13]3[S:14][CH:15]=[C:16]([C:18](OCC)=[O:19])[N:17]=3)=[C:8]2[C:7](=[O:31])[N:6]([CH3:32])[C:5]1=[O:33].[Cl-].[Li+]>C(O)C.C1COCC1>[OH:19][CH2:18][C:16]1[N:17]=[C:13]([C:12]2[N:11]([CH2:23][O:24][CH2:25][CH2:26][Si:27]([CH3:29])([CH3:28])[CH3:30])[CH:10]=[C:9]3[C:8]=2[C:7](=[O:31])[N:6]([CH3:32])[C:5](=[O:33])[N:4]3[CH3:3])[S:14][CH:15]=1

参加物

6

実験手順

Sodium borohydride (0.856 g, 22.62 mmol) was added to a solution of ethyl 2-(1,3-dimethyl-2,4-dioxo-6-((2-(trimethylsilyl)ethoxy)methyl)-2,3,4,6-tetrahydro-1H-pyrrolo[3,4-d]pyrimidin-5-yl)thiazole-4-carboxylate (step 1) (5.254 g, 11.31 mmol) and lithium chloride (0.959 g, 22.62 mmol) in ethanol (145 ml) and THF (290 ml) at 0° C. The mixture was stirred at room temperature for 16 hours. Further portions of lithium chloride (0.959 g, 22.62 mmol) and sodium borohydride (0.856 g, 22.62 mmol) were added and the mixture stirred for a further 4 hours. The reaction was quenched with saturated NaHCO3 (aq) (250 ml), diluted with water (100 ml) and extracted with chloroform (3×350 ml). The combined organic extracts were washed with water (200 ml) and brine (2×200 ml), dried over sodium sulfate and evaporated under vacuum to afford the title compound.

後処理

  1. stirringthe mixture stirred for a further 4 hours
  2. customThe reaction was quenched with saturated NaHCO3 (aq) (250 ml)
  3. additiondiluted with water (100 ml)
  4. extractionextracted with chloroform (3×350 ml)
  5. washThe combined organic extracts were washed with water (200 ml) and brine (2×200 ml)
  6. dry with materialdried over sodium sulfate
  7. customevaporated under vacuum

出典と根拠

ORDレコード
ord-b2e8b866623b46e08cb575720495bdc5
出典データセット
uspto-grants-2016_06
特許番号
US09359381B2

反応ノート

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