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Morpholine → 6-(Morpholin-4-yl)pyridin-2-amine

HRID 1504762
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HRID 1504762 반응식
Cl[C:2]1[N:7]=[C:6]([NH2:8])[CH:5]=[CH:4][CH:3]=1.[NH:9]1[CH2:14][CH2:13][O:12][CH2:11][CH2:10]1>[Cl-].[NH4+].C(Cl)Cl>[N:9]1([C:2]2[N:7]=[C:6]([NH2:8])[CH:5]=[CH:4][CH:3]=2)[CH2:14][CH2:13][O:12][CH2:11][CH2:10]1
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참가 물질

5

반응물 2

HCID 8083MorpholineHCID 2062462-Amino-6-chloropyridine

생성물 1

HCID 187718606-(Morpholin-4-yl)pyridin-2-amine

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 25517Ammonium Chloride용매

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온도
200 °C

실험 절차

6-Chloropyridin-2-amine (244 mg, 1.90 mmol) and morpholine (0.827 mL, 9.49 mmol) were combined and heated for 2 hr at 200° C. via microwave irradiation. The reaction mixture was diluted with saturated aqueous ammonium chloride and DCM. The organics were separated, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel chromatography (10-80% acetone/hexanes, linear gradient) to afford 6-(morpholin-4-yl)pyridin-2-amine. MS ESI calc'd. for C9H14N3O [M+H]+ 180. found 180. 1H NMR (500 MHz, CDCl3) δ 7.29 (t, J=7.9 Hz, 1H), 5.99 (d, J=8.1 Hz, 1H), 5.91 (d, J=7.8 Hz, 1H), 3.82-3.75 (m, 4H), 3.46-3.38 (m, 4H).

후처리

  1. customThe organics were separated
  2. dry with materialdried over sodium sulfate
  3. concentrationconcentrated under reduced pressure
  4. customThe residue was purified by silica gel chromatography (10-80% acetone/hexanes, linear gradient)

출처 및 근거

ORD 기록
ord-f2efc2b2736d4c7ba34858ce17e8400f
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09216173B2

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