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Methylamine → HCID 484059, 화합물

HRID 369218
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HRID 369218 반응식
[CH3:1][NH2:2].[NH2:3][C:4]1[C:5]([F:28])=[CH:6][C:7]([F:27])=[C:8]([N:10]2[C:19]3[C:14](=[CH:15][C:16]([F:22])=[C:17](F)[C:18]=3[CH3:20])[C:13](=[O:23])[C:12]([C:24]([OH:26])=[O:25])=[CH:11]2)[CH:9]=1>N1C=CC=CC=1>[NH2:3][C:4]1[C:5]([F:28])=[CH:6][C:7]([F:27])=[C:8]([N:10]2[C:19]3[C:14](=[CH:15][C:16]([F:22])=[C:17]([NH:2][CH3:1])[C:18]=3[CH3:20])[C:13](=[O:23])[C:12]([C:24]([OH:26])=[O:25])=[CH:11]2)[CH:9]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6329MethylamineHCID 11132289HCID 11132289, 화합물

생성물 1

HCID 484059HCID 484059, 화합물

시약·촉매·용매 1

HCID 1049Pyridine용매

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온도
70 °C

실험 절차

Pyridine (200 mg) and a 40% aqueous solution (250 mg) of methylamine were added to 1(5-amino-2,4-difluorophenyl)-6,7-difluoro-8-methyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (100 mg), arid the mixture was heated and stirred overnight at 70° C. After the solvent was distilled off under reduced pressure, and ethanol (2 ml) and acetic acid (1 drop) were added to the residue to stir the mixture, solids deposited were collected by filtration and washed successively with ethanol and diethyl ether to obtain the title compound (51 mg) as a pale brown powder.

후처리

  1. temperaturewas heated
  2. distillationAfter the solvent was distilled off under reduced pressure, and ethanol (2 ml) and acetic acid (1 drop)
  3. additionwere added to the residue
  4. stirringto stir the mixture, solids
  5. filtrationdeposited were collected by filtration
  6. washwashed successively with ethanol and diethyl ether

출처 및 근거

ORD 기록
ord-63fd49dba7a4453a899c5c1f791dd636
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06136823

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