4-azido-N-(4-methylpyrimidin-2-yl)benzenesulfonamide

Base Information

• Chemical Name: 4-azido-N-(4-methylpyrimidin-2-yl)benzenesulfonamide
• CAS No.: 88609-05-6
• Molecular Formula: C₁₁H₁₀N₆O₂S
• Molecular Weight: 290.305
• NSC Number: 208410,84464
• DSSTox Substance ID: DTXSID50390569
• Wikidata: Q82187438
• ChEMBL ID: CHEMBL1742146

Synonyms:NSC84464;NSC-84464;88609-05-6;NCGC00013884;NCIStruc1_000584;NCIStruc2_000450;CHEMBL1742146;DTXSID50390569;NCI84464;CCG-36350;NSC208410;NSC-208410;NCGC00013884-02;NCGC00096994-01;NCI60_041859;N-(4-methyl-2-pyrimidinyl)-4-(25-1,2-triazadienyl)benzenesulfonamide

Chemical Property of 4-azido-N-(4-methylpyrimidin-2-yl)benzenesulfonamide

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Density: g/cm³
• XLogP3: 1.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 4
• Exact Mass: 290.05859476
• Heavy Atom Count: 20
• Complexity: 462

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=NC(=NC=C1)NS(=O)(=O)C2=CC=C(C=C2)N=[N+]=[N-]

Technology Process of 4-azido-N-(4-methylpyrimidin-2-yl)benzenesulfonamide

There total 1 articles about 4-azido-N-(4-methylpyrimidin-2-yl)benzenesulfonamide 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: 80.0%

sulfamerazina (127-79-7) → 4-azido-N-(4-methylpyrimidin-2-yl)benzenesulfonamide (88609-05-6)

Guidance literature:

sulfamerazina; With hydrogenchloride; sodium nitrite; In water; at 0 ℃; for 0.25h;

With sodium azide; In water; at 0 ℃;

DOI:10.1134/S1068162020030024

Reference yield:

4-azido-N-(4-methylpyrimidin-2-yl)benzenesulfonamide (88609-05-6) + 2-propynyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside (211688-84-5) → 4-{4-[(β-D-galactopyranosyl)oxymethyl]-1H-1,2,3-triazol-1-yl}-N-(4-methylpyrimidin-2-yl)benzenesulfonamide

Guidance literature:

Multi-step reaction with 2 steps

1: sodium L-ascorbate; copper(II) sulfate / N,N-dimethyl-formamide / 0.67 h / 70 °C / Microwave irradiation; Sealed tube

2: sodium methylate / methanol / 0 °C / pH 9

With sodium methylate; copper(II) sulfate; sodium L-ascorbate; In methanol; N,N-dimethyl-formamide;

DOI:10.5935/0103-5053.20140158

upstream raw materials:

sulfamerazina

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