Hexane → HCID 22873202, compound

HRID 1683171Notes

Reaction equation

HRID 1683171 reaction equation
[CH3:1][C@@:2]1(/[CH:28]=[CH:29]/[C:30]2[N:34]=[CH:33][O:32][N:31]=2)[S:8](=[O:10])(=[O:9])[C@H:7]2[N:4]([C:5](=[O:11])[CH2:6]2)[C@H:3]1[C:12]([O:14]C(C1C=CC=CC=1)C1C=CC=CC=1)=[O:13].CCCCCC>C1C(O)=CC=CC=1C>[CH3:1][C@@:2]1(/[CH:28]=[CH:29]/[C:30]2[N:34]=[CH:33][O:32][N:31]=2)[S:8](=[O:9])(=[O:10])[C@H:7]2[N:4]([C:5](=[O:11])[CH2:6]2)[C@H:3]1[C:12]([OH:14])=[O:13]

Participants

4

Conditions

Temperature
50 °C

Procedure

355 mg (0.74 mmol) of benzhydryl (E)-(2S,3S,5R)-3-methyl-3-[2-(1,2,4-oxadiazol-3-yl)-vinyl]-4,4,7-trioxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylate were dissolved in 3 ml of m-cresol and stirred at 50° C. for 4 hours. 20 ml of n-hexane are added to the pale brown solution, the separated crystals were filtered off under suction and rinsed with n-hexane. The crude crystallizate was recrystallized from ethyl acetate/n-hexane.

Workup

  1. filtrationthe separated crystals were filtered off under suction
  2. washrinsed with n-hexane
  3. customThe crude crystallizate was recrystallized from ethyl acetate/n-hexane

Sources & evidence

ORD record
ord-cb929a1e26fb4059a3c60f828038ada8
Source dataset
uspto-grants-1997_06
Patent number
US05637579

Reaction notes

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