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Stannous chloride dihydrate → 2-{2-[6-Amino-7-chloro-3-(3,5-dimethylphenyl)-2-oxo-1,2-dihydroquinolin-4-yloxy]-ethyl}-piperidine-1-carboxylic acid benzyl ester

HRID 1858065
ノート
印刷プレビュー

反応式

HRID 1858065 の反応式
O.O.[Sn](Cl)Cl.[CH2:6]([O:13][C:14]([N:16]1[CH2:21][CH2:20][CH2:19][CH2:18][CH:17]1[CH2:22][CH2:23][O:24][C:25]1[C:34]2[C:29](=[CH:30][C:31]([Cl:38])=[C:32]([N+:35]([O-])=O)[CH:33]=2)[NH:28][C:27](=[O:39])[C:26]=1[C:40]1[CH:45]=[C:44]([CH3:46])[CH:43]=[C:42]([CH3:47])[CH:41]=1)=[O:15])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>>[CH2:6]([O:13][C:14]([N:16]1[CH2:21][CH2:20][CH2:19][CH2:18][CH:17]1[CH2:22][CH2:23][O:24][C:25]1[C:34]2[C:29](=[CH:30][C:31]([Cl:38])=[C:32]([NH2:35])[CH:33]=2)[NH:28][C:27](=[O:39])[C:26]=1[C:40]1[CH:45]=[C:44]([CH3:46])[CH:43]=[C:42]([CH3:47])[CH:41]=1)=[O:15])[C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 61436Stannous chloride dihydrateHCID 544370152-{2-[6-Nitro-7-chloro-3-(3,5-dimethylphenyl)-2-oxo-1,2-dihydroquinolin-4-yloxy]-ethyl}-piperidine-1-carboxylic acid benzyl ester

生成物 1

HCID 539323332-{2-[6-Amino-7-chloro-3-(3,5-dimethylphenyl)-2-oxo-1,2-dihydroquinolin-4-yloxy]-ethyl}-piperidine-1-carboxylic acid benzyl ester収率 47.5%

反応条件

温度
70 °C

実験手順

To a solution of 2-{2-[6-nitro-7-chloro-3-(3,5-dimethylphenyl)-2-oxo-1,2-dihydroquinolin-4-yloxy]-ethyl}-piperidine-1-carboxylic acid benzyl ester (1.11 g in 30 mL ethanol) was added 2 mL tin(II)cloride dihydrate and the mixture heated to 70° C. on an oil bath. After 2 hours, the reaction was cooled to room temperature and quenched by the addition of 300 mL ice-water. The acidity of the resulting solution was adjusted to pH 8 by the addition of saturated aqueous sodium bicarbonate and the mixture extracted (2×) with ethyl acetate. The combined organics were washed with brine, dried over sodium sulfate and concentrated in vacuo. Purification of the crude oil by flash chromatography on silica gel (methylene chloride:ethyl acetate, 95:5) gave the title compound (0.50 g).

後処理

  1. temperaturethe reaction was cooled to room temperature
  2. customquenched by the addition of 300 mL ice-water
  3. additionThe acidity of the resulting solution was adjusted to pH 8 by the addition of saturated aqueous sodium bicarbonate
  4. extractionthe mixture extracted (2×) with ethyl acetate
  5. washThe combined organics were washed with brine
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated in vacuo
  8. customPurification of the crude oil by flash chromatography on silica gel (methylene chloride:ethyl acetate, 95:5)

出典と根拠

ORDレコード
ord-c94891cedfb349a58afe944a0e16e198
出典データセット
uspto-grants-2000_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06150352

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート