반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:12]([CH3:13])[N:11]=[CH:10][C:9]=2[CH:14]=O)=[CH:4][CH:3]=1.C(O)(=O)[CH2:17][C:18]([OH:20])=[O:19].N1CCCCC1.[OH-].[Na+]>C1(C)C=CC=CC=1.COCCOCCOC>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[N:12]([CH3:13])[N:11]=[CH:10][C:9]=2/[CH:14]=[CH:17]/[C:18]([OH:20])=[O:19])=[CH:6][CH:7]=1참가 물질
반응 조건
- 온도
- 92.5 °C
실험 절차
To a mixture of 5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehyde (3.00 g), malonic acid (1.99 g) and bis(2-methoxyethyl) ether (9 mL) was added dropwise piperidine (1.89 mL) over about 10 min. The mixture was stirred at 90-95° C. for 1 hr. and further at 105-110° C. for 4 hrs. After cooling to 25° C., toluene (12 mL) and 1N aqueous sodium hydroxide solution (15 mL) were added and the mixture was stirred. The aqueous layer was separated and the organic layer was extracted with 1N aqueous sodium hydroxide solution (6 mL). The aqueous layers were combined and washed with toluene. The layers were adjusted to pH 3.5-4.0 with 2N hydrochloric acid at 20-30° C. and water (9 mL) was added dropwise. After stirring at 25° C. for 1 hr., the precipitated crystals were collected by filtration and washed with 20% ethanol to give (2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]acrylic acid (3.24 g, yield 90%).
후처리
- waitand further at 105-110° C. for 4 hrs
- temperatureAfter cooling to 25° C.
- stirringthe mixture was stirred
- customThe aqueous layer was separated
- extractionthe organic layer was extracted with 1N aqueous sodium hydroxide solution (6 mL)
- washwashed with toluene
- customwere adjusted to pH 3.5-4.0 with 2N hydrochloric acid at 20-30° C.
- additionwater (9 mL) was added dropwise
- stirringAfter stirring at 25° C. for 1 hr
- filtration, the precipitated crystals were collected by filtration
- washwashed with 20% ethanol
출처 및 근거
- ORD 기록
- ord-db6aa61893614edf9ca87b9570f1139c
- 출처 데이터셋
- uspto-grants-2008_09
- 특허 번호
- US07423159B2
연결된 노트
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