Acetic Anhydride → 1-Methylethyl 5-(phenylmethoxy)-1H-indazole-3-carboxylate

HRID 1604630ノート

反応式

HRID 1604630 の反応式
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

6

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

  1. stirringthe mixture was stirred at same temperature for 4 hours
  2. temperatureAfter cooling
  3. filtrationinsoluble mass was filtered off
  4. concentrationthe filtrate was concentrated under reduced pressure
  5. dissolutionThe residue was dissolved in isopropyl alcohol (30 ml)
  6. additioncontaining conc. sulphuric acid (0.5 ml)
  7. stirringthe mixture was stirred at 80° C. for 3 hours
  8. temperatureAfter cooling to room temperatures the resulting crystals
  9. filtrationwere collected by filtration
  10. 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

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