Hydrochloric Acid → HCID 15280418、化合物
反応式
[C:1]([O-:15])(=O)[CH2:2][CH2:3][NH:4][C:5](=[O:13])[C@@H:6]([C:8]([CH2:11][OH:12])([CH3:10])[CH3:9])[OH:7].[Na+].[CH2:17]([NH2:20])[CH:18]=[CH2:19].Cl.C(OP(C#N)(=O)OCC)C.C(N(CC)CC)C>O.CN(C=O)C>[NH4+:4].[OH-:7].[CH2:17]([NH:20][C:1](=[O:15])[CH2:2][CH2:3][NH:4][C:5](=[O:13])[C@@H:6]([C:8]([CH2:11][OH:12])([CH3:9])[CH3:10])[OH:7])[CH:18]=[CH2:19]参加物
実験手順
To a solution of sodium pantothenate (10.0 g, 41.5 mmol) and allylamine (3.20 mL, 2.44 g, 42.6 mmol) in 50 mL of water was added 7.1 mL of concentrated aqueous HCl The resulting mixture (pH 2.0-2.5) was concentrated to afford a viscous syrup. The syrup was diluted with 50 mL of DMF, cooled in an ice bath, and treated with diethylcyanophosphonate (6.40 mL, 6.88 g, 42.2 mmol, 1.02 eq.) followed by triethylamine (13.0 mL, 9.44 g, 93.3 mmol, 2.25 equiv). The mixture was stirred at 0°-10° C. for 1 h and then concentrated. The residue was diluted with 200 mL of ethyl acetate and filtered. The filtrate was concentrated and the residue was chromatographed on a 5×27 cm silica gel column, eluting first with 85:14:1 CHCl3EtOH:aq NH4OH and then with 77.5:21:1.5 CHCl3 :EtOH:aq NH4OH to afford 8.03 g (75%) of pantothenic acid allyl amide as a pale yellow oil: TLC (85:14:1 CHCl3 :EtOH:aq NH4OH) Rf 0.40; 1H NMR (D2O) ∂5.83 (1, m), 5.17 (1H, m) 5.13 (1H, m), 3.96 (1H, s), 3.77 (2H, m), 3.51 (2H, m), 3,49 (1H, d, J=11.4 Hz), 3.37 (1H, d, J=11.4 Hz), 2.51 (2H, t, J=6.4 Hz), 0.90 (3H, s), 0.86 (3H, s).
後処理
- concentrationwas concentrated
- customto afford a viscous syrup
- temperaturecooled in an ice bath
- concentrationconcentrated
- additionThe residue was diluted with 200 mL of ethyl acetate
- filtrationfiltered
- concentrationThe filtrate was concentrated
- customthe residue was chromatographed on a 5×27 cm silica gel column
- washeluting first with 85:14:1 CHCl3EtOH
出典と根拠
- ORDレコード
- ord-0cab0c8499c2427da0e12dd9ec3c2a26
- 出典データセット
- uspto-grants-1995_03
- 特許番号
- US05401880
反応ノート
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