N-(3,4-dichlorophenyl)-[3-(2-hydroxypropyl)[1,2,4]-thiadiazol-5-yl]amine

Base Information

Chemical Name:N-(3,4-dichlorophenyl)-[3-(2-hydroxypropyl)[1,2,4]-thiadiazol-5-yl]amine
CAS No.:1275515-22-4
Molecular Formula:C₁₁H₁₁Cl₂N₃OS
Molecular Weight:304.2
Hs Code.:

Synonyms:N-(3,4-dichlorophenyl)-[3-(2-hydroxypropyl)[1,2,4]-thiadiazol-5-yl]amine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-(3,4-dichlorophenyl)-[3-(2-hydroxypropyl)[1,2,4]-thiadiazol-5-yl]amine

Chemical Property:

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Technology Process of N-(3,4-dichlorophenyl)-[3-(2-hydroxypropyl)[1,2,4]-thiadiazol-5-yl]amine

There total 4 articles about N-(3,4-dichlorophenyl)-[3-(2-hydroxypropyl)[1,2,4]-thiadiazol-5-yl]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:

: 726160-27-6
N-(3,4-dichlorophenyl)-[3-(2-oxopropyl)[1,2,4]-thiadiazol-5-yl]amine

: 1275515-22-4
N-(3,4-dichlorophenyl)-[3-(2-hydroxypropyl)[1,2,4]-thiadiazol-5-yl]amine

Guidance literature:: With sodium tetrahydroborate; In methanol; at 50 ℃;
DOI:10.1134/S0012500810120013

Reference yield:

: 321309-33-5
5-methylisoxazolyl-3-isothiocyanate

: 1275515-22-4
N-(3,4-dichlorophenyl)-[3-(2-hydroxypropyl)[1,2,4]-thiadiazol-5-yl]amine

Guidance literature:: Multi-step reaction with 2 steps

1: acetonitrile / Reflux

2: sodium tetrahydroborate / methanol / 0.5 h

With sodium tetrahydroborate; In methanol; acetonitrile;
DOI:10.1021/mp300011r

Reference yield:

: 6590-94-9
3,4-dichlorophenyl isothiocyanate

: 1275515-22-4
N-(3,4-dichlorophenyl)-[3-(2-hydroxypropyl)[1,2,4]-thiadiazol-5-yl]amine

Guidance literature:: Multi-step reaction with 2 steps

1: toluene-4-sulfonic acid / acetonitrile / Reflux

2: sodium tetrahydroborate; methanol / 50 °C

With methanol; sodium tetrahydroborate; toluene-4-sulfonic acid; In acetonitrile;