p-methoxybenzyl 3-(imidazo[1,2-b]pyridazine-6-yl)thio-7β-phenylacetylamino-3-cephem-4-carboxylate

Base Information

• Chemical Name: p-methoxybenzyl 3-(imidazo[1,2-b]pyridazine-6-yl)thio-7β-phenylacetylamino-3-cephem-4-carboxylate
• CAS No.: 342811-88-5
• Molecular Formula: C₂₉H₂₅N₅O₅S₂
• Molecular Weight: 587.68
• Mol file: 342811-88-5.mol

Synonyms:p-methoxybenzyl 3-(imidazo[1,2-b]pyridazine-6-yl)thio-7β-phenylacetylamino-3-cephem-4-carboxylate

Chemical Property of p-methoxybenzyl 3-(imidazo[1,2-b]pyridazine-6-yl)thio-7β-phenylacetylamino-3-cephem-4-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of p-methoxybenzyl 3-(imidazo[1,2-b]pyridazine-6-yl)thio-7β-phenylacetylamino-3-cephem-4-carboxylate

There total 3 articles about p-methoxybenzyl 3-(imidazo[1,2-b]pyridazine-6-yl)thio-7β-phenylacetylamino-3-cephem-4-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 81.0%

(7R)-7-[(phenylacetyl)amino]-3-trifluoromethanesulfonyloxy-3-cephem-4-carboxylate, 4-methoxybenzyl ester (123054-30-8) + sodium imidazo[1,2-b]pyridazine-6-thiolate → p-methoxybenzyl 3-(imidazo[1,2-b]pyridazine-6-yl)thio-7β-phenylacetylamino-3-cephem-4-carboxylate (342811-88-5)

Guidance literature:

In N,N-dimethyl-formamide; at 5 ℃; for 0.5h;

DOI:10.7164/antibiotics.54.257

Reference yield:

p-methoxybenzyl 7β-phenylacetylamino-3-hydroxy-3-cephem-4-carboxylate (123054-31-9) → p-methoxybenzyl 3-(imidazo[1,2-b]pyridazine-6-yl)thio-7β-phenylacetylamino-3-cephem-4-carboxylate (342811-88-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 5.95 mg / diisopropylethylamine / CH₂Cl₂ / 0.5 h / -78 °C

2: 81 percent / dimethylformamide / 0.5 h / 5 °C

With N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide;

DOI:10.7164/antibiotics.54.257

Reference yield:

6-chloroimidazo[1,2-b]pyridazine (6775-78-6) → p-methoxybenzyl 3-(imidazo[1,2-b]pyridazine-6-yl)thio-7β-phenylacetylamino-3-cephem-4-carboxylate (342811-88-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 90 percent / NaOMe / methanol / 3 h / 80 °C

2: 81 percent / dimethylformamide / 0.5 h / 5 °C

With sodium methylate; In methanol; N,N-dimethyl-formamide;

DOI:10.7164/antibiotics.54.257

upstream raw materials:

(7R)-7-[(phenylacetyl)amino]-3-trifluoromethanesulfonyloxy-3-cephem-4-carboxylate, 4-methoxybenzyl ester

p-methoxybenzyl 7β-phenylacetylamino-3-hydroxy-3-cephem-4-carboxylate

6-chloroimidazo[1,2-b]pyridazine