Methanol → HCID 178418456、化合物
反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[C:6]([OH:18])=[C:7]3[C:15](=[O:16])[NH:14][NH:13][C:12](=[O:17])[C:8]3=[N:9][C:10]=2[CH:11]=1.[OH-].[OH:20][CH2:21][CH2:22][N+:23]([CH3:26])([CH3:25])[CH3:24].C1(C)C=CC=CC=1.CO>O>[OH:20][CH2:21][CH2:22][N+:23]([CH3:26])([CH3:25])[CH3:24].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[C:6]([OH:18])=[C:7]3[C:15](=[O:16])[NH:14][NH:13][C:12](=[O:17])[C:8]3=[N:9][C:10]=2[CH:11]=1参加物
実験手順
To a stirred suspension of 7-chloro-2,3-dihydro-10-hydroxypyridazino[4,5-b]quinoline-1,4-dione (1.00 g, 3.8 mM) in water (40 mL) was added choline hydroxide (0.86 mL, 3.8 mM, 50 weight per cent, aqueous solution). Toluene (250 mL) was added to the resulting solution and the mixture was concentrated using a rotary evaporator. The residue was diluted with toluene (250 mL) and the resulting mixture concentrated again to provide a yellow residue. This residue was stirred for 60 hr with methanol (25 mL) and the resulting suspension was filtered to separate the solids which were washed with methanol (3 mL) and then dried under a stream of nitrogen for 1 hr. Further drying of the solids in vacuo at 100° C. for 20 hr provided (0.76 g, 55%) of the title compound as a yellow powder, mp 267°-269° C.
後処理
- concentrationthe mixture was concentrated
- customa rotary evaporator
- additionThe residue was diluted with toluene (250 mL)
- concentrationthe resulting mixture concentrated again
- customto provide a yellow residue
- filtrationthe resulting suspension was filtered
- customto separate the solids which
- washwere washed with methanol (3 mL)
- customdried under a stream of nitrogen for 1 hr
- customFurther drying of the solids in vacuo at 100° C. for 20 hr
出典と根拠
- ORDレコード
- ord-4061f90aaff7419f9113b9addf8ac370
- 出典データセット
- uspto-grants-1998_03
- 特許番号
- US05733910
反応ノート
読み込み中…