Diethylamine → HCID 58478769、化合物

HRID 1011342ノート

反応式

HRID 1011342 の反応式
[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

  1. extractionThe aqueous layer is extracted twice with EtOAc (2×)
  2. customThe combined organic extracts are dried
  3. concentrationconcentrated
  4. customThe residue is chromatographed (silica gel, EtOAc/hexane)
  5. additionThe product containing fractions
  6. 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

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