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Methanol → [1-(2-Phenylethylsulfonyl)piperidin-4-yl]methanamine

HRID 1351540
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HRID 1351540 반응식
C(OC(=O)[NH:10][CH2:11][CH:12]1[CH2:17][CH2:16][N:15]([S:18]([CH:21]=[CH:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)(=[O:20])=[O:19])[CH2:14][CH2:13]1)C1C=CC=CC=1.CO.[H][H]>[OH-].[Pd+2].[OH-].O1CCCC1>[C:23]1([CH2:22][CH2:21][S:18]([N:15]2[CH2:14][CH2:13][CH:12]([CH2:11][NH2:10])[CH2:17][CH2:16]2)(=[O:19])=[O:20])[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 887MethanolHCID 69413281[1-(2-Phenyl-ethenesulfonyl)-piperidin-4-ylmethyl]-carbamic acid benzyl esterHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 22135729[1-(2-Phenylethylsulfonyl)piperidin-4-yl]methanamine

시약·촉매·용매 2

HCID 9942167Palladium hydroxide촉매
HCID 8028
Tetrahydrofuran
용매

실험 절차

A mixture of [1-(2-phenyl-ethenesulfonyl)-piperidin-4-ylmethyl]-carbamic acid benzyl ester (2.5 g), 20% palladium hydroxide (1 g) on carbon, 200 mL of methanol and 50 mL of tetrahydrofuran were shaken under 50 psi of hydrogen for 2 days at room temperature. The catalyst was filtered off and washed with 250 mL of methanol. Concentration under reduced pressure gave C-[1-(2-phenyl-ethanesulfonyl)-piperidin-4-yl]-methylamine as white solid.

후처리

  1. filtrationThe catalyst was filtered off
  2. washwashed with 250 mL of methanol
  3. concentrationConcentration under reduced pressure

출처 및 근거

ORD 기록
ord-e29d215dc4814d65ba6e7c991cbeac03
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07217716B2

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