Pyridine → benzhydryl (6R,7R)-3-methyl-8-oxo-7-[(2-phenoxyacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

HRID 1758825

反応式

HRID 1758825 の反応式
[C:1]1([CH:7]([O:14][C:15]([C@@H:17]2[N:21]3[C:22](=[O:35])[C@@H:23]([NH:24]C(=O)COC4C=CC=CC=4)[C@H:20]3[S@@:19](=O)[C:18]2([CH3:38])[CH3:37])=[O:16])[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.N1C=[CH:43][CH:42]=[CH:41][CH:40]=1.C(Br)(=O)C.[O:49]1[CH2:54][CH2:53][O:52][CH2:51][CH2:50]1>>[C:8]1([CH:7]([O:14][C:15]([C:17]2[N:21]3[C:22](=[O:35])[C@@H:23]([NH:24][C:54](=[O:49])[CH2:53][O:52][C:51]4[CH:50]=[CH:43][CH:42]=[CH:41][CH:40]=4)[C@H:20]3[S:19][CH2:37][C:18]=2[CH3:38])=[O:16])[C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1

参加物

5

反応物 4

HCID 1049PyridineHCID 10482Acetyl bromideHCID 312751,4-DioxaneHCID 56631626Benzhydryl penicillin V sulfoxide, (S)-

生成物 1

HCID 112091benzhydryl (6R,7R)-3-methyl-8-oxo-7-[(2-phenoxyacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

反応条件

温度
100 °C

実験手順

(1S,3S,5R,6R) 2,2-Dimethyl-6-phenoxyacetamidopenam-3-carboxylic acid-1-oxide diphenylmethyl ester (25.00 gms, 45.41 mmoles) was dissolved in sieve-dried, peroxide-free dioxane (250 mls) at 25° C. with good agitation. To this solution, in order, were added pyridine (10.99 mls, 10.78 gms, 136.22 mmoles), acetyl bromide (0.67 mls, 1.12 gms, 9.08 mmoles) and dimethylsilyl diisocyanate (16.14 gms, 113.51 mmoles), and the slurry was heated to reflux (ca. 100° C.) for 4 hours. The dioxane slurry was then cooled to 25° C., filtered, and concentrated in vacuo at 50° C. to a heavy oil. The oil was taken up in methylene chloride (400 mls), stirred for 15 minutes at 25° C., filtered, and concentrated in vacuo to dryness. The residue was dissolved in hot 1-butanol (500 mls, ca. 90°-95° C.) and allowed to cool to 25° C. The slurry was cooled to 0°-5° C. for 16 hours, filtered, washed with cold butanol (0°-5° C., 100 mls), then with Skellysolve B (200 mls), and oven-dried at 45° C. to constant weight. Yield: 20.2 gms, 86.4% of snow-white crystalline title compound. The NMR spectrum was clean and consistent for the desired structure, as follows: 80 MHz H' NMR, δ(CD2Cl2) 2.08 (3H,s,CH3), 3.04-3.62 (2H, m, CH2, JAB =18.1 Hz), 4.55 (2H, s, CH2), 4.99-5.05 (1H, d, β-lactam H, JA =4.7 Hz), 5.74-5.91 (1 H, m, β-lactam H, J=4.7 Hz), 6.75-7.50 (17H, m, aromatic CH, and NH).

後処理

  1. customin sieve-dried
  2. customat 25° C.
  3. temperaturethe slurry was heated
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo at 50° C. to a heavy oil
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo to dryness
  8. dissolutionThe residue was dissolved in hot 1-butanol (500 mls, ca. 90°-95° C.)
  9. temperatureto cool to 25° C
  10. temperatureThe slurry was cooled to 0°-5° C. for 16 hours
  11. filtrationfiltered
  12. washwashed with cold butanol (0°-5° C., 100 mls)
  13. dry with materialwith Skellysolve B (200 mls), and oven-dried at 45° C. to constant weight

出典と根拠

ORDレコード
ord-e0e87b34dca14214933ae63e4d79aa6a
出典データセット
uspto-grants-1983_02
特許番号
US04374982

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