Hydrochloric Acid → HCID 15280418, 화합물

HRID 1609771노트

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HRID 1609771 반응식
[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]

참가 물질

9

실험 절차

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).

후처리

  1. concentrationwas concentrated
  2. customto afford a viscous syrup
  3. temperaturecooled in an ice bath
  4. concentrationconcentrated
  5. additionThe residue was diluted with 200 mL of ethyl acetate
  6. filtrationfiltered
  7. concentrationThe filtrate was concentrated
  8. customthe residue was chromatographed on a 5×27 cm silica gel column
  9. washeluting first with 85:14:1 CHCl3EtOH

출처 및 근거

ORD 기록
ord-0cab0c8499c2427da0e12dd9ec3c2a26
출처 데이터셋
uspto-grants-1995_03
특허 번호
US05401880

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