HCID 12834167, compound → HCID 12834098, compound

HRID 1764018Notes

Reaction equation

HRID 1764018 reaction equation
[CH3:1][CH:2]1[CH:7]=[C:6]([C:8]([OH:10])=[O:9])[N:5]2[C:11](=[O:32])[CH:12]([NH:13][C:14](=[O:31])[CH:15]([C:25]3[CH2:26][O:27][CH2:28][CH2:29][CH:30]=3)[NH:16]C(OC(C3CC3)C)=O)[C@H:4]2[S:3]1>C(O)=O>[CH3:1][CH:2]1[CH:7]=[C:6]([C:8]([OH:10])=[O:9])[N:5]2[C:11](=[O:32])[CH:12]([NH:13][C:14](=[O:31])[CH:15]([C:25]3[CH2:26][O:27][CH2:28][CH2:29][CH:30]=3)[NH2:16])[C@H:4]2[S:3]1

Participants

3

Reactant 1

HCID 12834167HCID 12834167, compound

Product 1

HCID 12834098HCID 12834098, compoundYield 96.6%

Reagents, catalysts & solvents 1

HCID 284Formic AcidSolvent

Procedure

A mixture of 2-methyl-7-[N-(Cl-cyclopropylethoxy)carbonyl-2-(5,6-dihydro-2H-pyran-3-yl)glycyl]amino-3-cephem-4-carboxylic acid (3.0 g) and formic acid (20 ml) was stirred for 3 hours at room temperature. After the reaction was completed, formic acid was removed from the reaction mixture under reduced pressure at room temperature. The residue was pulverized with acetonitrile and the powder was collected by filtration. The powder was in turn washed with acetonitrile and water, and dried to give 2-methyl-7-[2-(5,6-dihydro-2H-pyran-3-yl)glycyl]amino-3-cephem-4-carboxylic acid (2.20 g), mp 125° to 128° C. (dec.).

Workup

  1. customformic acid was removed from the reaction mixture under reduced pressure at room temperature
  2. filtrationthe powder was collected by filtration
  3. washwashed with acetonitrile and water
  4. customdried

Sources & evidence

ORD record
ord-57313b76b1f94944aa26a89fb1fde08e
Source dataset
uspto-grants-1978_09
Patent number
US04113940

Reaction notes

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