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HCID 10861009, 화합물 → 4-Cyclohexyl-4-[(1H-1,2,4-triazol-1-yl)methyl]piperidine

HRID 1795176
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반응식

HRID 1795176 반응식
C(OC([N:8]1[CH2:13][CH2:12][C:11]([CH:20]2[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]2)([CH2:14][N:15]2[CH:19]=[N:18][CH:17]=[N:16]2)[CH2:10][CH2:9]1)=O)(C)(C)C>FC(F)(F)C(O)=O.ClCCl.O>[CH:20]1([C:11]2([CH2:14][N:15]3[CH:19]=[N:18][CH:17]=[N:16]3)[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]2)[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 10861009HCID 10861009, 화합물

생성물 1

HCID 129914504-Cyclohexyl-4-[(1H-1,2,4-triazol-1-yl)methyl]piperidine

시약·촉매·용매 1

HCID 18672661TFA dichloromethane water용매

실험 절차

To a solution of trifluoroacetic acid/dichloromethane/water (1:1:0.1, 10 mL) is added 4-cyclohexyl-4-[1,2,4]triazole-1-ylmethyl-piperidine-1-carboxylic acid tert-butyl ester, 3, (3.5 g, 10 mmol) which was obtained in the procedure herein above and the reaction mixture is allowed to stir for 30 to 60 minutes. The reaction solution is then concentrated in vacuo and partitioned between aqueous NaHCO3 and EtOAc. The organic phase is concentrated in vacuo and the crude product purified by HPLC over silica gel to afford the desired product.

후처리

  1. custom(3.5 g, 10 mmol) which was obtained in the procedure herein above and the reaction mixture
  • concentrationThe reaction solution is then concentrated in vacuo
  • custompartitioned between aqueous NaHCO3 and EtOAc
  • concentrationThe organic phase is concentrated in vacuo
  • customthe crude product purified by HPLC over silica gel
  • 출처 및 근거

    ORD 기록
    ord-489934a29b7f46258165e4134c0f57d2
    출처 데이터셋
    uspto-grants-2006_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07026335B2

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