Diethylamine → HCID 58478769、化合物
反応式
[O:1]=[C:2]1[C:10]2[C:5](=[N:6][C:7]([CH:11]=O)=[CH:8][CH:9]=2)[CH2:4][O:3]1.[CH2:13]([NH:15][CH2:16][CH3:17])[CH3:14].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C([O-])(O)=O.[Na+]>ClC(Cl)C>[CH2:13]([N:15]([CH2:11][C:7]1[N:6]=[C:5]2[CH2:4][O:3][C:2](=[O:1])[C:10]2=[CH:9][CH:8]=1)[CH2:16][CH3:17])[CH3:14]参加物
6
実験手順
A solution of 5-oxo-5,7-dihydro-furo[3,4-b]pyridine-2-carbaldehyde (110 mg, 0.68 mmol) in dichloroethane (4 mL) is treated with diethylamine (75 μL, 0.68 mmol) followed by the addition of sodium triacetoxyborohydride (200 mg, 0.94 mmol). The reaction mixture is stirred at room temperature for 1.5 h. and then treated with saturated aqueous NaHCO3 solution. The aqueous layer is extracted twice with EtOAc (2×). The combined organic extracts are dried, and concentrated. The residue is chromatographed (silica gel, EtOAc/hexane). The product containing fractions are concentrated to give the title compound as white solid (90 mg, 61%).
後処理
- extractionThe aqueous layer is extracted twice with EtOAc (2×)
- customThe combined organic extracts are dried
- concentrationconcentrated
- customThe residue is chromatographed (silica gel, EtOAc/hexane)
- additionThe product containing fractions
- concentrationare concentrated
出典と根拠
- ORDレコード
- ord-5ac5fd0297df46b0915bdba4d48d5a02
- 出典データセット
- uspto-grants-2011_07
- 特許番号
- US07977351B2
反応ノート
読み込み中…