4-([1,3]Thiazolo[5,4-b]pyridin-2-yl)aniline

Base Information

• Chemical Name: 4-([1,3]Thiazolo[5,4-b]pyridin-2-yl)aniline
• CAS No.: 121717-35-9
• Molecular Formula: C12H9N3S
• Molecular Weight: 227.29
• DSSTox Substance ID: DTXSID30366702
• Wikidata: Q82152064
• Mol file: 121717-35-9.mol

Synonyms:121717-35-9;4-(thiazolo[5,4-b]pyridin-2-yl)aniline;4-([1,3]thiazolo[5,4-b]pyridin-2-yl)aniline;(4-[1,3]Thiazolo[5,4-{b}]pyridin-2-ylphenyl)amine;4-{[1,3]thiazolo[5,4-b]pyridin-2-yl}aniline;F1694-0005;DTXSID30366702;HMS1654I19;AKOS005208431;EN300-237808;SR-01000014316;SR-01000014316-1

Chemical Property of 4-([1,3]Thiazolo[5,4-b]pyridin-2-yl)aniline

Chemical Property:

• PSA: 80.04000
• LogP: 3.52170
• XLogP3: 2.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 227.05171847
• Heavy Atom Count: 16
• Complexity: 240

Purity/Quality:

NLT 98% ^*data from raw suppliers

(4-[1,3]Thiazolo[5,4-{b}]pyridin-2-ylphenyl)amine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC2=C(N=C1)SC(=N2)C3=CC=C(C=C3)N

Technology Process of 4-([1,3]Thiazolo[5,4-b]pyridin-2-yl)aniline

There total 4 articles about 4-([1,3]Thiazolo[5,4-b]pyridin-2-yl)aniline 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: 65.0%

2-(p-nitrophenyl)thiazolo<5,4-b>pyridine (121717-37-1) → 2-(p-aminophenyl)thiazolo<5,4-b>pyridine (121717-35-9)

Guidance literature:

With sodium hydrogensulfide; In methanol; water; for 6h; Heating;

Reference yield:

2-chloro-3-aminopyridine (6298-19-7) → 2-(p-aminophenyl)thiazolo<5,4-b>pyridine (121717-35-9)

Guidance literature:

Multi-step reaction with 3 steps

1: pyridine

2: 71 percent / Lawesson's reagent / hexamethylphosphoric acid triamide / 3 h / 140 °C

3: 65 percent / sodium hydrogen sulfide / methanol; H₂O / 6 h / Heating

With Lawessons reagent; pyridine; sodium hydrogensulfide; In methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; water;

Reference yield:

N-(2-Chloro-pyridin-3-yl)-4-nitro-benzamide (121311-55-5) → 2-(p-aminophenyl)thiazolo<5,4-b>pyridine (121717-35-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 71 percent / Lawesson's reagent / hexamethylphosphoric acid triamide / 3 h / 140 °C

2: 65 percent / sodium hydrogen sulfide / methanol; H₂O / 6 h / Heating

With Lawessons reagent; sodium hydrogensulfide; In methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; water;

upstream raw materials:

2-(p-nitrophenyl)thiazolo<5,4-b>pyridine

2-chloro-3-aminopyridine

N-(2-Chloro-pyridin-3-yl)-4-nitro-benzamide

4-nitro-benzoyl chloride

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