烯胺
产量(工程)
盐酸盐
催化作用
配体(生物化学)
化学
组合化学
胍
不对称氢化
有机化学
对映选择合成
材料科学
生物化学
受体
冶金
作者
Melissa Birch,Stephen Challenger,Jean-Philippe Crochard,David Fradet,Hayley Jackman,Amy Luan,Evelyn Madigan,Jinu S. Mathew,Neil McDowall,Kevin Meldrum,Charles M. Gordon,Philip Peach,Stephen Yeo
摘要
The development of a highly efficient two-step process for the manufacture of the α2δ-ligand imagabalin hydrochloride 1 is described in 50% overall yield from (R)-3-methylhexanoic acid 2. Key aspects of this route include the development of a one-pot process for the synthesis of β-enamine ester 7 and its subsequent diastereoselective hydrogenation with a Ru-(S)-BINAP catalyst. The use of a combination of TFA, ammonium trifluoroacetate, and relatively low pressures in the asymmetric hydrogenation are novel conditions reported for this type of transformation. The simplified process described realised a 4-fold reduction in cost of goods compared with the previously described enabling route.
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