C-(2-METHYL-IMIDAZO[2,1-B]THIAZOL-6-YL)-METHYLAMINE

Base Information

• Chemical Name: C-(2-METHYL-IMIDAZO[2,1-B]THIAZOL-6-YL)-METHYLAMINE
• CAS No.: 518064-25-0
• Molecular Formula: C7H9N3S
• Molecular Weight: 167.235
• Hs Code.: 2934100090
• Mol file: 518064-25-0.mol

Synonyms:C-(2-METHYL-IMIDAZO[2,1-B]THIAZOL-6-YL)-METHYLAMINE;1-(2-methylimidazo[2,1-b][1,3]thiazol-6-yl)methanamine(SALTDATA: FREE);(2-methylimidazo[2,1-b]thiazol-6-yl)methanamine

Chemical Property of C-(2-METHYL-IMIDAZO[2,1-B]THIAZOL-6-YL)-METHYLAMINE

Chemical Property:

• PSA: 71.56000
• Density: 1.46g/cm³
• LogP: 1.86320

Purity/Quality:

98% ^*data from raw suppliers

1-(2-methylimidazo[2,1-b][1,3]thiazol-6-yl)methanaminedihydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of C-(2-METHYL-IMIDAZO[2,1-B]THIAZOL-6-YL)-METHYLAMINE

There total 1 articles about C-(2-METHYL-IMIDAZO[2,1-B]THIAZOL-6-YL)-METHYLAMINE 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: 97.0%

6-(azidomethyl)-2-methylimidazo[2,1-b][1,3]thiazole (891845-29-7) → 1-(2-methylimidazo[2,1-b][1,3]thiazol-6-yl)methanamine (518064-25-0)

Guidance literature:

With hydrogen; palladium 10% on activated carbon; In methanol; at 20 ℃; under 760.051 Torr;

Reference yield: 86.0%

Fmoc-Tyr(tBu)-OH (71989-38-3,118488-18-9,204384-67-8) + 1-(2-methylimidazo[2,1-b][1,3]thiazol-6-yl)methanamine (518064-25-0) → O-(1,1-dimethylethyl)-N-{[(9H-fluoren-9-ylmethyl)oxy]carbonyl}-N-[(2-methylimidazo[2,1-b][1,3]thiazol-6-yl)methyl]-L-tyrosinamide (891845-30-0)

Guidance literature:

With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20 ℃; for 3h; Inert atmosphere;

DOI:10.1021/jm800634k

Reference yield: 77.0%

Boc-Tyr(t-Bu)-OH (47375-34-8) + 1-(2-methylimidazo[2,1-b][1,3]thiazol-6-yl)methanamine (518064-25-0) → O-(1,1-dimethylethyl)-N-{[(1,1-dimethylethyl)oxy]carbonyl}-N-[(2-methylimidazo[2,1-b][1,3]thiazol-6-yl)methyl]-L-tyrosinamide (891845-36-6)

Guidance literature:

With HATU; diisopropyl-carbodiimide; In N,N-dimethyl-formamide; at 20 ℃; for 3h;

upstream raw materials:

6-(azidomethyl)-2-methylimidazo[2,1-b][1,3]thiazole

Downstream raw materials:

O-(1,1-dimethylethyl)-N-{[(1,1-dimethylethyl)oxy]carbonyl}-N-[(2-methylimidazo[2,1-b][1,3]thiazol-6-yl)methyl]-L-tyrosinamide

O-(1,1-dimethylethyl)-N-{[(9H-fluoren-9-ylmethyl)oxy]carbonyl}-N-[(2-methylimidazo[2,1-b][1,3]thiazol-6-yl)methyl]-L-tyrosinamide

6-[(2R)-2-(2,5-difluorophenyl)pyrrolidin-yl]-N-[(2-methylimidazo[2,1-b][1,3]thiazol-6-yl)methyl]pyrido[3,2-d]pyrimidin-4-amine

Refernces

• 1、 -. "QUATERNARY AMMONIUM SALTS OF FUSED HETEAROMATIC AMINES AS NOVEL MUSCARINIC ACETYLCHOLINE RECEPTOR ANTAGONISTS". Page/Page column 10; 11; 14. . Retrieved 2010/11/08.