Sodium hydride → (S)-2-tert-Butoxycarbonylamino-3-(3-methyl-oxetan-3-ylmethoxy)-propionic acid

HRID 2285414ノート

反応式

HRID 2285414 の反応式
[C:1]([O:5][C:6]([NH:8][C@H:9]([C:12]([OH:14])=[O:13])[CH2:10][OH:11])=[O:7])([CH3:4])([CH3:3])[CH3:2].[H-].[Na+].Br[CH2:18][C:19]1([CH3:23])[CH2:22][O:21][CH2:20]1>CS(C)=O>[C:1]([O:5][C:6]([NH:8][C@@H:9]([CH2:10][O:11][CH2:18][C:19]1([CH3:23])[CH2:22][O:21][CH2:20]1)[C:12]([OH:14])=[O:13])=[O:7])([CH3:4])([CH3:2])[CH3:3]

参加物

5

反応物 3

HCID 24758Sodium hydride2 回HCID 98766N-[tert-butoxycarbonyl]-L-serineHCID 144860Oxetane, 3-(bromomethyl)-3-methyl-

生成物 1

HCID 86709710(S)-2-tert-Butoxycarbonylamino-3-(3-methyl-oxetan-3-ylmethoxy)-propionic acid収率 63%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

To N-(tert-Butoxycarbonyl)-L-serine (1.2 g, 6.06 mmol) in anhydrous dimethyl sulfoxide (20 mL) at room temperature and under an atmosphere of nitrogen was added sodium hydride (60% in mineral oil, 363 mg, 9.1 mmol) in three portions. The reaction was stirred for 1 h after which was added 3-bromomethyl-3-methyl oxetane (obtained from Fluorochem Ltd., UK), 1 g, 6.06 mmol) and a further amount of sodium hydride (60% in mineral oil, 363 mg, 9.1 mmol). The reaction was stirred for 16 h and quenched by careful addition of water. The solution was washed with diethyl ether (1×) and acidified to pH 2 with 2 M hydrochloric acid. The solution was extracted with ethyl acetate (2×) and the combined organics washed with brine. The organic layer was dried through a hydrophobic frit and concentrated in vacuo to yield the title compound (1.1 g, 63%) as a clear oil. 1H NMR (300 MHz, CDCl3) δ 1.30 (s, 3H), 1.48 (s, 9H), 3.50, 3.53 (ABq, J=9.4 Hz, 2H), 3.77 (dd, J=9.4, 3.8 Hz, 1H), 3.98 (dd, J=9.4, 2.9 Hz, 1H), 4.37 (d, J=5.8 Hz, 2H), 4.47-4.55 (m, 1H), 4.57 (d, J=5.8 Hz, 2H), 5.47 (d, J=8.3 Hz, 1H). LCMS (m/z) 289.3 [M+H], Tr=1.67 min.

後処理

  1. stirringThe reaction was stirred for 16 h
  2. customquenched by careful addition of water
  3. washThe solution was washed with diethyl ether (1×)
  4. extractionThe solution was extracted with ethyl acetate (2×)
  5. washthe combined organics washed with brine
  6. customThe organic layer was dried through a hydrophobic frit
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-1b209d54dd324401a5a0fd4a9d2bab89
出典データセット
uspto-grants-2015_09
特許番号
US09145441B2

反応ノート

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