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Ammonia → HCID 57588245, 화합물

HRID 15024
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HRID 15024 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 222AmmoniaHCID 57588246HCID 57588246, 화합물

생성물 1

HCID 57588245HCID 57588245, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A mixture of intermediate (45) (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 (46).

후처리

  1. filtration
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
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
  • 출처 및 근거

    ORD 기록
    ord-fd536bce10cb4c4f8dde1767a7b76ec6
    출처 데이터셋
    uspto-grants-2010_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07732464B2

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