Ethyl 2-(benzylamino)-1,3-thiazole-4-carboxylate

Base Information

• Chemical Name: Ethyl 2-(benzylamino)-1,3-thiazole-4-carboxylate
• CAS No.: 126534-13-2
• Molecular Formula: C₁₃H₁₄N₂O₂S
• Molecular Weight: 262.332
• European Community (EC) Number: 899-266-6
• ChEMBL ID: CHEMBL3593865
• Nikkaji Number: J3.448.078H
• Mol file: 126534-13-2.mol

Synonyms:126534-13-2;ethyl 2-(benzylamino)-1,3-thiazole-4-carboxylate;CHEMBL3593865;SCHEMBL10467196;JLSAVNDMVKWSPJ-UHFFFAOYSA-N;AKOS017259500;MS-9588;Ethyl 2-benzylaminothiazole-4-carboxylate;CS-0298987;Ethyl 2-(benzylamino)thiazole-4-carboxylate;AB00769115-01;Ethyl 4-(benzylamino)-3,5-thiazolecarboxylate, 95%;Z48849908;Ethyl 2-(benzylimino)-2,3-dihydrothiazole-4-carboxylate

Chemical Property of Ethyl 2-(benzylamino)-1,3-thiazole-4-carboxylate

Chemical Property:

• XLogP3: 3.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 6
• Exact Mass: 262.07759887
• Heavy Atom Count: 18
• Complexity: 270

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CCOC(=O)C1=CSC(=N1)NCC2=CC=CC=C2

Technology Process of Ethyl 2-(benzylamino)-1,3-thiazole-4-carboxylate

There total 2 articles about Ethyl 2-(benzylamino)-1,3-thiazole-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: 75.0%

ethyl Bromopyruvate (70-23-5) + N-benzylthiourea (621-83-0) → ethyl 2-(benzylamino)thiazole-4-carboxylate (126534-13-2)

Guidance literature:

In ethanol; Reflux;

DOI:10.1021/acs.jmedchem.5b00226

Reference yield:

→ ethyl 2-(N-phenylamino)thiazole-4-carboxylate (126533-76-4) + ethyl 2-(benzylamino)thiazole-4-carboxylate (126534-13-2)

Guidance literature:

Reference yield:

ethyl 2-(benzylamino)thiazole-4-carboxylate (126534-13-2) → 2-benzylaminothiazol-4-ylmethanol + 2-tritylaminothiazole-4-methanol (126533-38-8)

Guidance literature:

In tetrahydrofuran;

upstream raw materials:

ethyl Bromopyruvate

N-benzylthiourea

Downstream raw materials:

2-tritylaminothiazole-4-methanol