Tributylphosphine → HCID 22624977、化合物
反応式
N(C(N1CCCCC1)=O)=NC(N1CCCCC1)=O.[ClH:19].[F:20][C:21]1[CH:40]=[C:39](C)[C:38]([O:42][C:43]([O:45][CH3:46])=[O:44])=[CH:37][C:22]=1[NH:23][C:24]1[C:33]2[C:28](=[CH:29][C:30]([OH:36])=[C:31]([O:34][CH3:35])[CH:32]=2)[N:27]=[CH:26][N:25]=1.C(P(CCCC)CCCC)CCC.O[CH2:61][CH2:62][CH2:63][C:64]1[CH:69]=[CH:68][N:67]=[CH:66][CH:65]=1>C(Cl)Cl>[Cl:19][C:39]1[C:38]([O:42][C:43]([O:45][CH3:46])=[O:44])=[CH:37][C:22]([NH:23][C:24]2[C:33]3[C:28](=[CH:29][C:30]([O:36][CH2:61][CH2:62][CH2:63][C:64]4[CH:69]=[CH:68][N:67]=[CH:66][CH:65]=4)=[C:31]([O:34][CH3:35])[CH:32]=3)[N:27]=[CH:26][N:25]=2)=[C:21]([F:20])[CH:40]=1参加物
実験手順
1,1'-(Azodicarbonyl)dipiperidine (2.52 g, 10 mmol) in methylene chloride (10 ml) was added dropwise to a solution of 4-(2-fluoro-5-methoxycarbonyloxy4-methylanilino)-7-hydroxy-6-methoxyquinazoline hydrochloride (1.38 g, 3.5 mmol), (prepared as described for the starting material in Example 22), tributylphosphine (2 g, 10.5 mmol). and 4-(3-hydroxypropyl)pyridine (720 mg, 5.25 mmol) in methylene chloride (25 ml) and the mixture stirred for 2.5 hours at ambient temperature. The solvent was removed by evaporation and the residue was triturated with petroleum ether. The solid product was collected by filtration and purified by column chromatography eluting with methylene chloride/methanol (95/5) to give 4-(4-chloro-2-fluoro-5-methoxycarbonyloxyanilino)-6-methoxy-7-(3-(4-pyridyl)propoxy)quinazoline (1.2 g, 67%).
後処理
- custom(prepared
- customThe solvent was removed by evaporation
- customthe residue was triturated with petroleum ether
- filtrationThe solid product was collected by filtration
- custompurified by column chromatography
- washeluting with methylene chloride/methanol (95/5)
出典と根拠
- ORDレコード
- ord-ef14717096c342d2af318e2762941684
- 出典データセット
- uspto-grants-2000_06
- 特許番号
- US06071921
反応ノート
読み込み中…