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Pyridine → HCID 86305571, 화합물

HRID 712595
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HRID 712595 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]2[CH:8]=[C:9]3[C:14](=[N:15][CH:16]=2)[NH:13][CH2:12][CH2:11][CH2:10]3)[CH:2]=1.N1C=CC=CC=1.[C:23](Cl)(=[O:25])[CH3:24].C([O-])(O)=O.[Na+]>C(Cl)Cl.O>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]2[CH:8]=[C:9]3[C:14](=[N:15][CH:16]=2)[N:13]([C:23](=[O:25])[CH3:24])[CH2:12][CH2:11][CH2:10]3)[CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 1049PyridineHCID 6367Acetyl chlorideHCID 516892Sodium BicarbonateHCID 117667315HCID 117667315, 화합물

생성물 1

HCID 86305571HCID 86305571, 화합물수율 76.9%

시약·촉매·용매 2

HCID 962Water용매
HCID 6344
Dichloromethane
용매

실험 절차

6-Pyridin-3-yl-1,2,3,4-tetrahydro-[1,8]naphthyridine (41 mg, 0.19 mmol) is dissolved in 2 mL of DCM and pyridine (0.19 mL, 2.3 mmol) is added into the solution. Then acetyl chloride (0.08 mL, 1.2 mmol) is added. The mixture is stirred for 0.5 hrs and saturated aqueous NaHCO3 (2 mL) is added along with water (3 mL). The mixture is extracted with EtOAc (3×10 mL) and the organic layers are combined and concentrated to give the crude product. Purification by flash column chromatography affords 37 mg of the titled product.

후처리

  1. extractionThe mixture is extracted with EtOAc (3×10 mL)
  2. concentrationconcentrated
  3. customto give the crude product
  4. customPurification by flash column chromatography

출처 및 근거

ORD 기록
ord-322f6ff0c8534feda80c7511dcc7602d
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181272B2

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