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Hydroxylamine → 1-tert-Butyloxycarbonyl-4-(N-Hydroxycarbamimidoyl)piperidine

HRID 2362660
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HRID 2362660 반응식
[C:1]([CH:3]1[CH2:8][CH2:7][N:6]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:5][CH2:4]1)#[N:2].[NH2:16][OH:17]>C(O)C>[OH:17]/[N:16]=[C:1](/[CH:3]1[CH2:8][CH2:7][N:6]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:5][CH2:4]1)\[NH2:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 787HydroxylamineHCID 1514443Tert-butyl 4-cyanopiperidine-1-carboxylate

생성물 1

HCID 219372541-tert-Butyloxycarbonyl-4-(N-Hydroxycarbamimidoyl)piperidine

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
80 °C

실험 절차

A solution of tert-butyl 4-cyanopiperidine-1-carboxylate (0.5 g, 2.378 mmol) in ethanol (12 mL) was treated with hydroxylamine (50% in water, 0.51 mL, 8.32 mmol). The reaction was heated at 80° C. for 1.5 hours. The reaction was cooled to ambient temperature and concentrated under reduced pressure. The concentrate was dried to constant weight in a vacuum oven at 60° C. to provide the title compound. DCI(+) m/z 244.1 [M+H]+.

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후처리

  1. temperatureThe reaction was cooled to ambient temperature
  2. concentrationconcentrated under reduced pressure
  3. customThe concentrate was dried to constant weight in a vacuum oven at 60° C.

출처 및 근거

ORD 기록
ord-8d4ac3ee3fd0461b9eaa10fb903c07b4
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08691810B2

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