Methylamine → 4-Chloro-N-methylpicolinamide

HRID 491062

반응식

HRID 491062 반응식
Cl.[Cl:2][C:3]1[CH:8]=[CH:7][N:6]=[C:5]([C:9](Cl)=[O:10])[CH:4]=1.[CH3:12][NH2:13]>C1COCC1.CO>[Cl:2][C:3]1[CH:8]=[CH:7][N:6]=[C:5]([C:9]([NH:13][CH3:12])=[O:10])[CH:4]=1

참가 물질

5

반응물 2

HCID 6329MethylamineHCID 223972704-Chloropyridine-2-carbonyl chloride--hydrogen chloride (1/1)

생성물 1

HCID 14768144-Chloro-N-methylpicolinamide

시약·촉매·용매 2

HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

실험 절차

4-Chloropyridine-2-carbonyl chloride HCl salt (7.0 g, 32.95 mmol) was added in portions to a mixture of a 2.0 M methylamine solution in THF (100 mL) and MeOH (20 mL) at 0° C. The resulting mixture was stored at 3° C. for 4 h, then concentrated under reduced pressure. The resulting nearly dry solids were suspended in EtOAc (100 mL) and filtered. The filtrate was washed with a saturated NaCl solution (2×100 mL), dried (Na2SO4) and concentrated under reduced pressure to provide 4-chloro-N-methyl-2-pyridinecarboxamide as a yellow, crystalline solid (4.95 g, 88%): mp 37-40° C.

후처리

  1. concentrationconcentrated under reduced pressure
  2. filtrationfiltered
  3. washThe filtrate was washed with a saturated NaCl solution (2×100 mL)
  4. dry with materialdried (Na2SO4)
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-5af6c5b34e184248a5fcbf2fdae5b2e5
출처 데이터셋
uspto-grants-2009_05
특허 번호
US07528255B2

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