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Benzyl-4-(benzyloxymethoxy)-4-(2-fluoro-2-methylpropyl)piperidine-1-carboxylate → 4-(2-Fluoro-2-methylpropyl)piperidin-4-ol

HRID 514863
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인쇄 미리보기

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HRID 514863 반응식
C(OC([N:11]1[CH2:16][CH2:15][C:14]([O:22]COCC2C=CC=CC=2)([CH2:17][C:18]([F:21])([CH3:20])[CH3:19])[CH2:13][CH2:12]1)=O)C1C=CC=CC=1>[Pd].CO>[F:21][C:18]([CH3:20])([CH3:19])[CH2:17][C:14]1([OH:22])[CH2:13][CH2:12][NH:11][CH2:16][CH2:15]1
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참가 물질

4

반응물 1

HCID 90418934Benzyl-4-(benzyloxymethoxy)-4-(2-fluoro-2-methylpropyl)piperidine-1-carboxylate

생성물 1

HCID 904190284-(2-Fluoro-2-methylpropyl)piperidin-4-ol

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a round bottom flask was added benzyl-4-(benzyloxymethoxy)-4-(2-fluoro-2-methylpropyl)piperidine-1-carboxylate (50 mg, 0.12 mmol), Pd/C (20 mg), and methanol (5 mL). The mixture was stirred at room temperature for 16 hrs under hydrogen atmosphere. The reaction mixture was filtered to get a solution, which was concentrated to give the desired product. The crude product was used directly for the next step. LC-MS: m/z 176.2 (M+H)+

후처리

  1. filtrationThe reaction mixture was filtered
  2. customto get a solution, which
  3. concentrationwas concentrated

출처 및 근거

ORD 기록
ord-beb09356dd5543eebe5f3336e6cd2731
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09108921B2

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