Acetic Anhydride → 1-Methylethyl 5-(phenylmethoxy)-1H-indazole-3-carboxylate
反応式
C([O-])(=O)C.[K+].[NH2:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[CH:9][C:8]=1[CH2:21][C:22]([O:24][CH:25]([CH3:27])[CH3:26])=[O:23].C(OC(=O)C)(=O)C.C(O[N:41]=O)CC(C)C>C1C=CC=CC=1>[CH2:14]([O:13][C:10]1[CH:9]=[C:8]2[C:7](=[CH:12][CH:11]=1)[NH:6][N:41]=[C:21]2[C:22]([O:24][CH:25]([CH3:27])[CH3:26])=[O:23])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1参加物
反応条件
- 温度
- 80 °C
実験手順
A mixture of potassium acetate (1.34 g), isopropyl 2-amino-5-benzyloxyphenylacetate (3.9 g) and acetic anhydride (4.0 g) in benzene (40 ml) was stirred at 80° C. After 30 minutes, isopentylnitrite (2.3 g) was added dropwise to the mixture over 15 minutes and then the mixture was stirred at same temperature for 4 hours. After cooling, insoluble mass was filtered off and the filtrate was concentrated under reduced pressure. The residue was dissolved in isopropyl alcohol (30 ml) containing conc. sulphuric acid (0.5 ml) and the mixture was stirred at 80° C. for 3 hours. After cooling to room temperatures the resulting crystals were collected by filtration and washed with isopropyl ether to give isopropyl 5-benzyloxy-1H-indazole-3-carboxylate (2.4 g).
後処理
- stirringthe mixture was stirred at same temperature for 4 hours
- temperatureAfter cooling
- filtrationinsoluble mass was filtered off
- concentrationthe filtrate was concentrated under reduced pressure
- dissolutionThe residue was dissolved in isopropyl alcohol (30 ml)
- additioncontaining conc. sulphuric acid (0.5 ml)
- stirringthe mixture was stirred at 80° C. for 3 hours
- temperatureAfter cooling to room temperatures the resulting crystals
- filtrationwere collected by filtration
- washwashed with isopropyl ether
出典と根拠
- ORDレコード
- ord-b5aca1c87310416d8e84518bd59f8223
- 出典データセット
- uspto-grants-1999_11
- 特許番号
- US05994378
反応ノート
読み込み中…