4-Methylmorpholine → HCID 90114235、化合物

HRID 2275899ノート

反応式

HRID 2275899 の反応式
[CH3:1][C:2]([NH2:8])([CH2:5][CH2:6][CH3:7])[CH2:3][NH2:4].[F:9][C:10]1[CH:31]=[CH:30][CH:29]=[C:28]([F:32])[C:11]=1[CH2:12][O:13][C:14]1[C:15]2[N:16]([C:21]([C:25](O)=[O:26])=[C:22]([CH3:24])[N:23]=2)[CH:17]=[C:18]([CH3:20])[CH:19]=1.CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.CN1CCOCC1>CN(C=O)C.O.C(O)(C(F)(F)F)=O>[NH2:8][C:2]([CH3:1])([CH2:5][CH2:6][CH3:7])[CH2:3][NH:4][C:25]([C:21]1[N:16]2[CH:17]=[C:18]([CH3:20])[CH:19]=[C:14]([O:13][CH2:12][C:11]3[C:28]([F:32])=[CH:29][CH:30]=[CH:31][C:10]=3[F:9])[C:15]2=[N:23][C:22]=1[CH3:24])=[O:26]

参加物

7

実験手順

77 mg (0.66 mmol) of rac-2-methylpentane-1,2-diamine were added to 200 mg (0.60 mmol) of 8-[(2,6-difluorobenzyl)oxy]-2,6-dimethylimidazo[1,2-a]pyridine-3-carboxylic acid Example 21A, 203 mg (0.63 mmol) of TBTU and 0.27 ml (2.41 mmol) of 4-methylmorpholine in DMF (2.1 ml), and the reaction mixture was stirred at RT overnight. The mixture was diluted with water/TFA and purified by preparative RP-HPLC (acetonitrile/water gradient with addition of 0.1% TFA). The product fraction was concentrated. Saturated aqueous sodium bicarbonate solution was added to the residue, and the mixture was extracted twice with dichloromethane. The combined organic phases were dried over sodium sulphate, filtered off and concentrated. This gave 199 mg (76% of theory, purity 99%) of the target compound.

後処理

  1. custompurified by preparative RP-HPLC (acetonitrile/water gradient with addition of 0.1% TFA)
  2. concentrationThe product fraction was concentrated
  3. additionSaturated aqueous sodium bicarbonate solution was added to the residue
  4. extractionthe mixture was extracted twice with dichloromethane
  5. dry with materialThe combined organic phases were dried over sodium sulphate
  6. filtrationfiltered off
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-83c101ffb9674bb8a7b17aa8a9c7e12e
出典データセット
uspto-grants-2015_09
特許番号
US09126998B2

反応ノート

読み込み中…