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Methyl iodide → HCID 178496655、化合物

HRID 243090
ノート
印刷プレビュー

反応式

HRID 243090 の反応式
[OH:1][C@@H:2]1[CH2:5][C@H:4]([NH:6][C:7](=[O:13])[O:8][C:9]([CH3:12])([CH3:11])[CH3:10])[CH2:3]1.[H-].[Na+].I[CH3:17]>C1COCC1>[C:9]([O:8][C:7](=[O:13])[NH:6][C@H:4]1[CH2:3][C@@H:2]([O:1][CH3:17])[CH2:5]1)([CH3:10])([CH3:12])[CH3:11]
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 6328Methyl iodideHCID 24758Sodium hydrideHCID 178454125HCID 178454125、化合物

生成物 1

HCID 178496655HCID 178496655、化合物収率 192.1%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

tert-Butyl (cis-3-hydroxycyclobutyl)carbamate (0.8 g, 4.3 mmol) was dissolved in dry THF (25 mL) under a nitrogen atmosphere, and the solution cooled to 0° C. To this clear solution, sodium hydride (60% dispersion in oil, 0.17 g, 4.3 mmol) was added portion wise (evolution of H2 observed). The mixture was stirred at RT for 30 min. then iodomethane (0.40 mL, 1.5 mmol) added dropwise and the resulting yellow suspension stirred at rt for 16 h. The reaction mixture was quenched with saturated aqueous solution of NH4Cl (20 mL) and partitioned between saturated aqueous solution of NaHCO3 (40 mL) and DCM (60 mL). The combined organic fractions were washed with brine (20 mL), dried (MgSO4) and concentrated in vacuo. The resulting residue was purified by column chromatography (gradient 0-70% EtOAc in cyclohexane) to afford the title compound as a white solid (0.58 g, 66%). 1H NMR (CDCl3, 300 MHz): δ 4.66 (1H, br, NH), 3.71-3.62 (1H, m), 3.61-3.50 (1H, m), 2.71 (3H, s), 2.76-1.62 (2H, m), 1.78-1.62 (2H, m), 1.41 (9H, s).

後処理

  1. stirringthe resulting yellow suspension stirred at rt for 16 h
  2. customThe reaction mixture was quenched with saturated aqueous solution of NH4Cl (20 mL)
  3. custompartitioned between saturated aqueous solution of NaHCO3 (40 mL) and DCM (60 mL)
  4. washThe combined organic fractions were washed with brine (20 mL)
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated in vacuo
  7. customThe resulting residue was purified by column chromatography (gradient 0-70% EtOAc in cyclohexane)

出典と根拠

ORDレコード
ord-be9c4b57e9c746adae149d78482c7ecb
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08653089B2

反応ノート

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