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Methanol → HCID 54112621、化合物

HRID 716129
ノート
印刷プレビュー

反応式

HRID 716129 の反応式
B(Cl)(Cl)Cl.[NH2:5][C:6]1[CH:11]=[CH:10][N:9]([CH:12]2[C@@H:16]([F:17])[C@H:15]([O:18]CC3C=CC(Cl)=CC=3)[C@@H:14]([CH2:27][O:28]CC3C=CC(Cl)=CC=3)[S:13]2)[C:8](=[O:37])[N:7]=1.CO>C(Cl)Cl>[NH2:5][C:6]1[CH:11]=[CH:10][N:9]([CH:12]2[S:13][C@H:14]([CH2:27][OH:28])[C@@H:15]([OH:18])[C@@H:16]2[F:17])[C:8](=[O:37])[N:7]=1
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

5

反応物 3

HCID 887MethanolHCID 25135Boron TrichlorideHCID 89975754HCID 89975754、化合物

生成物 1

HCID 54112621HCID 54112621、化合物収率 72.4%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

反応条件

温度
0 °C

実験手順

In a nitrogen atmosphere, 6.8 mL of a methylene chloride solution of 1 mol/L boron trichloride was added to a solution of 0.17 g of (3S,4S,5R)-2-(4-amino-2-oxo-1,2-dihydropyrimidin-1-yl)-4-((4-chlorobenzyl)oxy)-5-(((4-chlorobenzyl)oxy)methyl)-3-fluorothiolane in 11 mL of methylene chloride under cooling on dry ice/acetone, and the obtained mixture was then stirred at the same temperature as described above for 3.5 hours. Thereafter, the temperature of the reaction mixture was increased to 0° C., and the reaction mixture was then stirred for 30 minutes. Thereafter, 7.5 mL of methanol was added to the reaction mixture, and the thus obtained mixture was then stirred at room temperature for 30 minutes. Thereafter, a solid was collected by filtration, and it was successively washed with ethyl acetate and hexane. The obtained solid was purified by silica gel column chromatography (chloroform/methanol=100/0 to 60/40), so as to obtain 63 mg of (2R,3S,4S)-5-(4-amino-2-oxo-1,2-dihydropyrimidin-1-yl)-4-fluoro-2-(hydroxymethyl)thiolan-3-ol in the form of a white solid.

後処理

  1. temperatureunder cooling on dry ice/acetone
  2. customas described above for 3.5 hours
  3. stirringthe reaction mixture was then stirred for 30 minutes
  4. stirringthe thus obtained mixture was then stirred at room temperature for 30 minutes
  5. filtrationThereafter, a solid was collected by filtration, and it
  6. washwas successively washed with ethyl acetate and hexane
  7. customThe obtained solid was purified by silica gel column chromatography (chloroform/methanol=100/0 to 60/40)

出典と根拠

ORDレコード
ord-50831cdb2df34ab8a92c021ac7220d98
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09187514B2

反応ノート

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