Phosphate → HCID 70547083、化合物

HRID 894383

反応式

HRID 894383 の反応式
[CH3:1][C:2]1([CH3:13])[C@H:6]([C:7]#[N:8])[N:5]2[C:9](=[O:12])[C@H:10](Br)[C@H:4]2[S:3]1.O1CCCCC1OC1C=CC(C=O)=CC=1.P([O-])([O-])([O-])=O>O1CCCC1.[Zn]>[CH3:1][C:2]1([CH3:13])[C@H:6]([C:7]#[N:8])[N:5]2[C:9](=[O:12])[CH2:10][C@H:4]2[S:3]1

参加物

6

実験手順

Activated mossy zinc (500 mg) and zinc dust (100 mg) are added to a solution of 2,2-dimethyl-3α-cyano-6α-bromopenam (522 mg, 2 mmol) and p-(2-tetrahydropyranyloxy)benzaldehyde (750 mg, 3.75 mmol) prepared according to E. Piers, W. deWaal and R. W. Britton, J. Am. Chem. Soc., 93, 5113 (1971) in 1 ml of dry tetrahydrofuran. After stirring vigorously at 50° for 3 hrs., the mixture is allowed to cool and 1 ml of pH 5 phosphate buffer is added. After standing for 10 min., the solids are removed by filtration and washed thoroughly with ethyl acetate. The filtrate is extracted with ethyl acetate. The combined extracts are washed with phosphate buffer and saturated sodium chloride, dried with sodium sulfate and the solvents removed by evaporation. The crude material is purified by chromatography on 60 g of silica gel using 40% acetone/chloroform as eluant to afford 2,2-dimethyl-3α-cyanopenam as a by-product melting at 73°- 75° C. and a mixture of 2,2-dimethyl-3α-cyano-6α-[p-(2-tetrahydropyranyloxy)-α-hydroxybenzyl]penam and 2,2-dimethyl-3α-cyano-6β-[p-(2-tetrahydropyranyloxy)-α-hydroxybenzyl]penam. Separation of the 6α- and 6β-compounds is effected by PLC (10% acetone/toluene; two developments) providing the individual 6α- and 6β-compounds.

後処理

  1. customprepared
  2. temperatureto cool
  3. waitAfter standing for 10 min.
  4. customthe solids are removed by filtration
  5. washwashed thoroughly with ethyl acetate
  6. extractionThe filtrate is extracted with ethyl acetate
  7. washThe combined extracts are washed with phosphate buffer and saturated sodium chloride
  8. dry with materialdried with sodium sulfate
  9. customthe solvents removed by evaporation
  10. customThe crude material is purified by chromatography on 60 g of silica gel using 40% acetone/chloroform as eluant

出典と根拠

ORDレコード
ord-577602433f524b5c8e6340992b1d1d70
出典データセット
uspto-grants-1981_08
特許番号
US04283531

関連ノート

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