反応式
Cl.[Br:2][C:3]1[N:7]2[CH:8]=[C:9]([C:12]([OH:14])=O)[N:10]=[CH:11][C:6]2=[CH:5][CH:4]=1.[C:15]1([NH2:26])[C:20](F)=[C:19](F)[C:18](F)=[C:17](N)C=1F.Cl.Cl.[CH3:29][CH2:30][N:31](C(C)C)C(C)C.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F>CN(C=O)C.C1COCC1>[N:26]12[CH2:17][CH2:18][CH:19]([CH2:20][CH2:15]1)[C@@H:30]([NH:31][C:12]([C:9]1[N:10]=[CH:11][C:6]3[N:7]([C:3]([Br:2])=[CH:4][CH:5]=3)[CH:8]=1)=[O:14])[CH2:29]2参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
To a suspension of 6-bromopyrrolo[1,2-a]pyrazine-3-carboxylic acid hydrochloride (1.67 mmol), (R)-3-aminoquinulidine dihydrochloride (0.34 g, 1.67 mmol), DIEA (1.5 mL, 8.35 mmol) in DMF (20 mL) and THF (10 mL) is added HATU (0.64 g, 1.67 mmol). The resulting suspension is stirred for 16 h at which time it is concentrated to dryness under reduced pressure. The resulting material is absorbed to silica gel and purified with silica gel chromatography (9% MeOH/1%NH3OH/CH2Cl2 as the eluent) salted with fumeric acid, and crystallized from EtOH/acetone/Et2O to give an off white spheres. Yield 45%. HRMS (FAB) calcd. for C15H17BrN4O+H 349.0664, found 349.0647.
後処理
- concentrationis concentrated to dryness under reduced pressure
- customThe resulting material is absorbed to silica gel
- custompurified with silica gel chromatography (9% MeOH/1%NH3OH/CH2Cl2 as the eluent)
- customcrystallized from EtOH/acetone/Et2O
- customto give an off white spheres
出典と根拠
- ORDレコード
- ord-719641f08ec94b06a39361fb8608fa61
- 出典データセット
- uspto-grants-2005_02
- 特許番号
- US06858613B2
関連ノート
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