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Chlorosuccinimide → 4-Chloro-2-methyl-2,6-naphthyridin-1-one

HRID 575611
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HRID 575611 반응식
[Cl:1]N1C(=O)CCC1=O.[CH3:9][N:10]1[CH:19]=[CH:18][C:17]2[C:12](=[CH:13][CH:14]=[N:15][CH:16]=2)[C:11]1=[O:20]>C(#N)C>[Cl:1][C:18]1[C:17]2[C:12](=[CH:13][CH:14]=[N:15][CH:16]=2)[C:11](=[O:20])[N:10]([CH3:9])[CH:19]=1
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참가 물질

4

반응물 2

HCID 31398ChlorosuccinimideHCID 210711812-methyl-2,6-naphthyridin-1(2H)-one

생성물 1

HCID 1180225434-Chloro-2-methyl-2,6-naphthyridin-1-one수율 56%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
65 °C

실험 절차

N-chlorosuccinimide (0.8 g, 6.2 mmol) was added in portions to a solution of 2-methyl-2,6-naphthyridin-1-one (1.0 g, 6.2 mmol) in acetonitrile (25 mL) which was then heated at 65° C. for 18 h. Extractive work up with ethyl acetate and purification by silica gel chromatography (PE:EA=5:1-1:1) gave the title compound of step 1 (0.6 g, 56%) as a yellow solid. 1H NMR: (CDCl3, 400 MHz) δ 9.29 (s, 1H), 8.81 (d, J=3.6 Hz, 1H), 8.21 (d, J=5.2 Hz, 1H), 7.31 (s, 1H), 3.63 (s, 3H). LCMS: 195.0 (M+H)+.

후처리

  1. customExtractive work up with ethyl acetate and purification by silica gel chromatography (PE:EA=5:1-1:1)

출처 및 근거

ORD 기록
ord-5d9ca800a72a4c3c97b30e198249ec5e
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09034900B2

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