Isopropanol → 4-[(3-Chloro-4-methoxybenzyl)amino]-1(4-hydroxypiperidino)-6-phthalazine carbothiamide

HRID 47346

反応式

HRID 47346 の反応式
P([O-])(OCC)(SCC)=[S:2].[Cl:10][C:11]1[CH:12]=[C:13]([CH:35]=[CH:36][C:37]=1[O:38][CH3:39])[CH2:14][NH:15][C:16]1[C:25]2[C:20](=[CH:21][CH:22]=[C:23]([C:26]#[N:27])[CH:24]=2)[C:19]([N:28]2[CH2:33]CCC[CH:29]2O)=[N:18][N:17]=1.[CH:40]([OH:43])([CH3:42])[CH3:41]>O>[Cl:10][C:11]1[CH:12]=[C:13]([CH:35]=[CH:36][C:37]=1[O:38][CH3:39])[CH2:14][NH:15][C:16]1[C:25]2[C:20](=[CH:21][CH:22]=[C:23]([C:26](=[S:2])[NH2:27])[CH:24]=2)[C:19]([N:28]2[CH2:33][CH2:42][CH:40]([OH:43])[CH2:41][CH2:29]2)=[N:18][N:17]=1

参加物

5

実験手順

3.7 ml diethyl dithiophosphate was added to a mixture of 2.0 g 4-[(3-chloro-4-methoxybenzyl)amino]-1-(hydroxypiperidino)-6-phthalazine carbonitrile, 1 ml water and 2 ml isopropanol, and the mixture was heated under reflux for 1 hr. After cooling, water was added to the reaction solution and the resulting crystals were collected by filtration. The filtrate was extracted with ethyl acetate and washed with brine. It was dried over anhydrous sodium sulfate, and filtered. The filtrate was evaporated, and the resulting crystalline residue was combined with the crystals collected above by filtration, whereby 1.5 g of the title compound was obtained.

後処理

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 1 hr
  3. temperatureAfter cooling
  4. filtrationthe resulting crystals were collected by filtration
  5. extractionThe filtrate was extracted with ethyl acetate
  6. washwashed with brine
  7. dry with materialIt was dried over anhydrous sodium sulfate
  8. filtrationfiltered
  9. customThe filtrate was evaporated
  10. filtrationcollected above by filtration

出典と根拠

ORDレコード
ord-5695479b783148a5bdc14f2c5cdf229d
出典データセット
uspto-grants-2004_03
特許番号
US06699870B2

関連ノート

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