5-(1-(4-chlorophenyl)-1H-tetrazol-5-ylsulfanylmethyl)-N-β-D-xylopyranosyl-1,3,4-thiadiazol-2-amine

Base Information

• Chemical Name: 5-(1-(4-chlorophenyl)-1H-tetrazol-5-ylsulfanylmethyl)-N-β-D-xylopyranosyl-1,3,4-thiadiazol-2-amine
• CAS No.: 1231978-34-9
• Molecular Formula: C₁₅H₁₆ClN₇O₄S₂
• Molecular Weight: 457.922
• Mol file: 1231978-34-9.mol

Synonyms:5-(1-(4-chlorophenyl)-1H-tetrazol-5-ylsulfanylmethyl)-N-β-D-xylopyranosyl-1,3,4-thiadiazol-2-amine

Chemical Property of 5-(1-(4-chlorophenyl)-1H-tetrazol-5-ylsulfanylmethyl)-N-β-D-xylopyranosyl-1,3,4-thiadiazol-2-amine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 5-(1-(4-chlorophenyl)-1H-tetrazol-5-ylsulfanylmethyl)-N-β-D-xylopyranosyl-1,3,4-thiadiazol-2-amine

There total 5 articles about 5-(1-(4-chlorophenyl)-1H-tetrazol-5-ylsulfanylmethyl)-N-β-D-xylopyranosyl-1,3,4-thiadiazol-2-amine 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: 68.0%

5-(1-(4-chlorophenyl)-1H-tetrazol-5-ylsulfanylmethyl)-N-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-1,3,4-thiadiazol-2-amine (1231978-16-7) → 5-(1-(4-chlorophenyl)-1H-tetrazol-5-ylsulfanylmethyl)-N-β-D-xylopyranosyl-1,3,4-thiadiazol-2-amine (1231978-34-9)

Guidance literature:

With methanol; sodium methylate; at 20 ℃; for 0.5h;

DOI:10.1016/j.carres.2011.01.010

Reference yield:

1-(4-chlorophenyl)-1H-tetrazole-5-thiol (27143-76-6) → 5-(1-(4-chlorophenyl)-1H-tetrazol-5-ylsulfanylmethyl)-N-β-D-xylopyranosyl-1,3,4-thiadiazol-2-amine (1231978-34-9)

Guidance literature:

Multi-step reaction with 5 steps

1: sodium hydroxide

2: hydrazine hydrate / ethanol / 4 h / Reflux

3: benzene / 4 h / Reflux

4: phosphoric acid; acetic anhydride / 24 h / 20 °C

5: methanol; sodium methylate / 0.5 h / 20 °C

With methanol; phosphoric acid; sodium methylate; acetic anhydride; hydrazine hydrate; sodium hydroxide; In ethanol; benzene;

DOI:10.1016/j.carres.2011.01.010

Reference yield:

<<1-(4-chlorophenyl)-1H-tetrazol-5-yl>thio>-acetic acid hydrazide (115781-88-9) → 5-(1-(4-chlorophenyl)-1H-tetrazol-5-ylsulfanylmethyl)-N-β-D-xylopyranosyl-1,3,4-thiadiazol-2-amine (1231978-34-9)

Guidance literature:

Multi-step reaction with 3 steps

1: benzene / 4 h / Reflux

2: phosphoric acid; acetic anhydride / 24 h / 20 °C

3: methanol; sodium methylate / 0.5 h / 20 °C

With methanol; phosphoric acid; sodium methylate; acetic anhydride; In benzene;

DOI:10.1016/j.carres.2011.01.010

upstream raw materials:

1-(4-chlorophenyl)-1H-tetrazole-5-thiol

N'-[N-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)thiocarbamoyl]-2-(1-(4-chlorophenyl)-1H-tetrazol-5-ylsulfanyl)acetohydrazide

5-(1-(4-chlorophenyl)-1H-tetrazol-5-ylsulfanylmethyl)-N-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-1,3,4-thiadiazol-2-amine

<<1-(4-chlorophenyl)-1H-tetrazol-5-yl>thio>-acetic acid hydrazide