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Ammonia → HCID 57588245、化合物

HRID 1993762
ノート
印刷プレビュー

反応式

HRID 1993762 の反応式
CC1C=CC(S(O[CH2:12][C@@H:13]2[CH2:18][CH2:17][N:16]([C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[CH2:15][C@H:14]2[O:26][CH3:27])(=O)=O)=CC=1.[NH3:28]>C1COCC1>[NH2:28][CH2:12][C@@H:13]1[CH2:18][CH2:17][N:16]([C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[CH2:15][C@H:14]1[O:26][CH3:27]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 222AmmoniaHCID 57588246HCID 57588246、化合物

生成物 1

HCID 57588245HCID 57588245、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A mixture of intermediate (49) (0.065 mol) in THF (250 ml) was treated with liquid NH3 in an autoclave at 125° C. during 16 hours. The reaction mixture was filtered and the filtrate was evaporated. The residue was partitioned between a 5% aqueous NaOH solution and DCM. The organic layer was separated, dried, filtered and the solvent was evaporated, yielding 16 g of 1,1-dimethylethyl (trans)-4-(aminomethyl)-3-methoxy-1-piperidinecarboxylate (intermediate (50).

後処理

filtration
The reaction mixture was filtered
  • customthe filtrate was evaporated
  • customThe residue was partitioned between a 5% aqueous NaOH solution and DCM
  • customThe organic layer was separated
  • customdried
  • filtrationfiltered
  • customthe solvent was evaporated
  • 出典と根拠

    ORDレコード
    ord-4c54869f80064c1aab3d533c9b8957d3
    出典データセット
    uspto-grants-2010_01
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07652040B2

    反応ノート

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