HCID 13457845, compound → HCID 178502814, compound

HRID 1761433Notes

Reaction equation

HRID 1761433 reaction equation
[NH2:1][C:2]1[S:3][CH:4]=[C:5](/[C:7](=[N:31]/[O:32][CH3:33])/[C:8]([NH:10][C@@H:11]2[C:29](=[O:30])[N:13]3[C:14]([C:26]([OH:28])=[O:27])=[C:15]([CH2:18]OC(=O)CC(=O)C)[CH2:16][S:17][C@H:12]23)=[O:9])[N:6]=1.[CH3:34][C:35]1[CH:40]=[CH:39][N:38]2[N:41]=[N:42][CH:43]=[C:37]2[CH:36]=1>>[NH2:1][C:2]1[S:3][CH:4]=[C:5](/[C:7](=[N:31]/[O:32][CH3:33])/[C:8]([NH:10][C@@H:11]2[C:29](=[O:30])[N:13]3[C:14]([C:26]([O-:28])=[O:27])=[C:15]([CH2:18][N:42]4[CH:43]=[C:37]5[CH:36]=[C:35]([CH3:34])[CH:40]=[CH:39][N:38]5[NH2+:41]4)[CH2:16][S:17][C@H:12]23)=[O:9])[N:6]=1

Participants

3

Reactant 2

HCID 13457845HCID 13457845, compoundHCID 21241316HCID 21241316, compound

Product 1

HCID 178502814HCID 178502814, compound

Procedure

7β-[2-(2-Aminothiazol-4-yl)-2(Z)-methoxyiminoacetamido]-3-(3-oxobutyryloxymethyl)-3-cephem-4-carboxylic acid and 5-methyl[1,2,3]triazolo[1,5-a]pyridine are treated by the same procedure as that in Example 1, to yield the desired compound.

Sources & evidence

ORD record
ord-53ff5be8681a4b6ba023cab86bbe56b1
Source dataset
uspto-grants-1989_05
Patent number
US04826834

Reaction notes

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