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Methanol → 1-Butyl-2-oxo-1,2-dihydropyridine-3-carboxylic acid

HRID 601156
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HRID 601156 반응식
[OH:1][C:2]1[N:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[OH-].[K+].CO.I[CH2:16][CH2:17][CH2:18][CH3:19]>O.Cl>[CH2:16]([N:10]1[CH:9]=[CH:8][CH:7]=[C:3]([C:4]([OH:6])=[O:5])[C:2]1=[O:1])[CH2:17][CH2:18][CH3:19]
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참가 물질

7

반응물 4

HCID 887MethanolHCID 10962Butyl iodideHCID 14797Potassium HydroxideHCID 178418543HCID 178418543, 화합물

생성물 1

HCID 227543301-Butyl-2-oxo-1,2-dihydropyridine-3-carboxylic acid수율 39%

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매
HCID 962
Water
용매
2회

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온도
60 °C

실험 절차

To a solution of 2-hydroxy-nicotinic acid (0.50 g, 3.59 mmol) and potassium -hydroxide (0.40 g, 7.13 mmol) in 4:1 methanol: water (6 mL) at room temperature, was added 1-iodobutane (0.74 mL, 6.42 mmol). This solution was heated at 60° C. for 30 minutes, then cooled to room temperature and diluted with water and 1N HCl. The resulting solid was filtered and dried to give the title compound (0.27 g, 39%). MS (DCI/NH3) m/z 196 (M+H)+; 1H NMR (300 MHz, DMSO-d6) δ 0.91 (m, 3 H) 1.30 (m, 2 H) 1.69 (m, 2 H) 4.10 (m, 2 H) 6.73 (m, 1 H) 8.27 (dd, J=6.62, 1.84 Hz, 1 H) 8.38 (dd, J=7.35, 2.21 Hz, 1 H) 14.68 (s, 1 H).

후처리

  1. temperaturecooled to room temperature
  2. filtrationThe resulting solid was filtered
  3. customdried

출처 및 근거

ORD 기록
ord-d8730e47c3c94c8081219799e8c83d5c
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07902203B2

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