Triethylamine → HCID 11258649、化合物
反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[C:9]([C:15](=[O:24])[C:16]1[CH:21]=[CH:20][CH:19]=[C:18]([O:22][CH3:23])[CH:17]=1)=[N:8][CH:7]=[C:6]2[C:25](O)=[O:26].C(N(CC)CC)C.C(OC(Cl)=O)C(C)C.C(O)(=O)/C=C/C(O)=O.[NH2:51][CH2:52][CH2:53][C:54]#[N:55].C(=O)(O)[O-].[Na+]>CN(C)C=O>[C:52]([CH2:53][CH2:54][NH:55][C:25]([C:6]1[C:5]2[C:10](=[CH:11][C:12]([O:13][CH3:14])=[C:3]([O:2][CH3:1])[CH:4]=2)[C:9]([C:15](=[O:24])[C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([O:22][CH3:23])[CH:17]=2)=[N:8][CH:7]=1)=[O:26])#[N:51]参加物
実験手順
A solution of 6,7-dimethoxy-1-(3-methoxy-benzoyl)-isoquinoline-4-carboxylic acid (170 mg, 0.46 mmol) in dry, N,N-dimethylformamide (5 mL) was chilled in an ice bath under argon. With stirring, triethylamine (97 uL, 0.69 mmol) and isobutylchloroformate (72 uL, 0.56 uL) were added. The solution was stirred for 30 min and then 3-aminopropionitrile fumarate (118 mg, 0.92 mmol) and triethylamine (250 uL, 1.79 mmol) were added. The solution was allowed to warmed to room temperature with stirring overnight. The reaction mixture was poured into a 2% aqueous sodium bicarbonate solution (50 mL) and extracted with ethyl acetate (3×25 mL). The combined ethyl acetate layers were dried over magnesium sulfate, filtered and concentrated in vacuo to afford 107 mg (55%) of an off white solid and used without further purification: APCI-MS m/e calcd for C23H21N3O5(M−H+) 420.4, found 420.0; 1H NMR (300 MHz) compatible.
後処理
- stirringThe solution was stirred for 30 min
- stirringwith stirring overnight
- extractionextracted with ethyl acetate (3×25 mL)
- dry with materialThe combined ethyl acetate layers were dried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customto afford 107 mg (55%) of an off white solid
- customused without further purification
出典と根拠
- ORDレコード
- ord-8dd6b8bc79f8489ea7b95f33350e8edf
- 出典データセット
- uspto-grants-2006_06
- 特許番号
- US07067529B2
反応ノート
読み込み中…