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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Carbamate → 2-Amino-N-methylpyridine-3-carboxamide

HRID 215685
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HRID 215685 반응식
[NH:1]1[C:6]2C=N[O:9][CH2:10][C:5]=2[C:4](=O)[CH2:3][C:2]1=O.C[NH2:14].[C:15](=O)([O-])[NH2:16].C(=O)=O>O1CCOCC1.C(O)C>[CH3:15][NH:16][C:10](=[O:9])[C:5]1[CH:4]=[CH:3][CH:2]=[N:1][C:6]=1[NH2:14]
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참가 물질

7

반응물 4

HCID 276CarbamateHCID 280Carbon DioxideHCID 6329MethylamineHCID 67131340HCID 67131340, 화합물

생성물 1

HCID 205853262-Amino-N-methylpyridine-3-carboxamide수율 97%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 312751,4-Dioxane용매

반응 조건

온도
40 °C

실험 절차

14.96 g (0.09 mol) of 1H-Pyrido[2,3-d]oxazin-2,4-dione was suspended in 138 ml dioxane. The mixture is heated to 40° C. and 17 ml of a 33% solution of methyl amine in ethanol is added dropwise directly into the reaction mixture, to avoid carbamate formation with the evolving CO2. The reaction is allowed to continue for 90 minutes. After cooling down to room temperature, the formed precipitate is removed by filtration and the filtrate is concentrated to dryness. 13.2 g (97%) of 2-aminonicotinic acid methyl amide was isolated (m.p. 140-2° C.).

후처리

  1. temperatureAfter cooling down to room temperature
  2. customthe formed precipitate is removed by filtration
  3. concentrationthe filtrate is concentrated to dryness

출처 및 근거

ORD 기록
ord-b2fff7c590ea4b8b851c57434f503c61
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08192918B2

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