benzyl 2-(4-((pyridin-2-ylmethylamino)methyl)benzoyl)-pyrazolidine-1-carboxylate

Base Information

• Chemical Name: benzyl 2-(4-((pyridin-2-ylmethylamino)methyl)benzoyl)-pyrazolidine-1-carboxylate
• CAS No.: 1059147-38-4
• Molecular Formula: C₂₅H₂₆N₄O₃
• Molecular Weight: 430.506
• Mol file: 1059147-38-4.mol

Synonyms:benzyl 2-(4-((pyridin-2-ylmethylamino)methyl)benzoyl)-pyrazolidine-1-carboxylate

Chemical Property of benzyl 2-(4-((pyridin-2-ylmethylamino)methyl)benzoyl)-pyrazolidine-1-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of benzyl 2-(4-((pyridin-2-ylmethylamino)methyl)benzoyl)-pyrazolidine-1-carboxylate

There total 5 articles about benzyl 2-(4-((pyridin-2-ylmethylamino)methyl)benzoyl)-pyrazolidine-1-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:

pyridine-2-carbaldehyde (1121-60-4) + benzyl 2-(4-(aminomethyl)benzoyl)pyrazolidine-1-carboxylate (1059147-36-2) → benzyl 2-(4-((pyridin-2-ylmethylamino)methyl)benzoyl)-pyrazolidine-1-carboxylate (1059147-38-4)

Guidance literature:

pyridine-2-carbaldehyde; benzyl 2-(4-(aminomethyl)benzoyl)pyrazolidine-1-carboxylate; In methanol; at 50 ℃; for 1.5h;

With sodium tetrahydroborate; In methanol; at 0 ℃; for 1h;

With water; sodium hydrogencarbonate; In methanol;

Reference yield:

benzyl pyrazolidine-1-carboxylate hydrochloride (57699-90-8) → benzyl 2-(4-((pyridin-2-ylmethylamino)methyl)benzoyl)-pyrazolidine-1-carboxylate (1059147-38-4)

Guidance literature:

Multi-step reaction with 3 steps

1.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 1 h / 0 °C

1.2: 18 h / 0 - 20 °C

2.1: trifluoroacetic acid / dichloromethane / 1.5 h / 20 °C

3.1: methanol / 1.5 h / 50 °C

3.2: 1 h / 0 °C

With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

1-tert-butoxycarbonyl-2-carbobenzyloxyhydrazine (57699-88-4) → benzyl 2-(4-((pyridin-2-ylmethylamino)methyl)benzoyl)-pyrazolidine-1-carboxylate (1059147-38-4)

Guidance literature:

Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 20 °C

1.2: 17 h / 20 °C

2.1: thionyl chloride / methanol / 16 h / 20 °C

3.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 1 h / 0 °C

3.2: 18 h / 0 - 20 °C

4.1: trifluoroacetic acid / dichloromethane / 1.5 h / 20 °C

5.1: methanol / 1.5 h / 50 °C

5.2: 1 h / 0 °C

With thionyl chloride; sodium hydride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In methanol; dichloromethane; N,N-dimethyl-formamide;

upstream raw materials:

pyridine-2-carbaldehyde

benzyl 2-(4-(aminomethyl)benzoyl)pyrazolidine-1-carboxylate

benzyl 2-(4-((tert-butoxycarbonyl)methyl)benzoyl)-pyrazolidine-1-carboxylate

1-tert-butoxycarbonyl-2-carbobenzyloxyhydrazine

Downstream raw materials:

benzyl 2-(4-((N-(pyridin-2-ylmethyl)phenylsulfonamido)-methyl)benzoyl)pyrazolidine-1-carboxylate

(4-((((1H-imidazol-2-yl)methyl)(pyridin-2-ylmethyl)amino)-methyl)phenyl)-(pyrazolidin-1-yl)methanone

N-(4-(pyrazolidine-1-carbonyl)benzyl)-N-(pyridin-2-ylmethyl)benzenesulfonamide

tert-butyl 4-(2-(4-((((1H-imidazol-2-yl)methyl)(pyridin-2-ylmethyl)amino)methyl)benzoyl)pyrazolidin-1-yl)-4-oxobutylcarbamate