4-{4-[(cyclohexyloxy)carbonyl]-1,3-thiazol-2-yl}piperidinium chloride

Base Information

Chemical Name:4-{4-[(cyclohexyloxy)carbonyl]-1,3-thiazol-2-yl}piperidinium chloride
CAS No.:1192247-99-6
Molecular Formula:C₁₅H₂₂N₂O₂S*ClH
Molecular Weight:330.879
Hs Code.:

Synonyms:4-{4-[(cyclohexyloxy)carbonyl]-1,3-thiazol-2-yl}piperidinium chloride

Suppliers and Price of 4-{4-[(cyclohexyloxy)carbonyl]-1,3-thiazol-2-yl}piperidinium chloride

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 4-{4-[(cyclohexyloxy)carbonyl]-1,3-thiazol-2-yl}piperidinium chloride

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-{4-[(cyclohexyloxy)carbonyl]-1,3-thiazol-2-yl}piperidinium chloride

There total 2 articles about 4-{4-[(cyclohexyloxy)carbonyl]-1,3-thiazol-2-yl}piperidinium chloride 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: 99.0%

: 1192247-97-4
tert-butyl 4-{4-[(cyclohexyloxy)carbonyl]-1,3-thiazol-2-yl}piperidine-1-carboxylate

: 1192247-99-6
4-{4-[(cyclohexyloxy)carbonyl]-1,3-thiazol-2-yl}piperidinium chloride

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; diethyl ether; at 0 - 20 ℃; Inert atmosphere;

Reference yield:

: 365413-31-6
ethyl 2-(1-(tert-butoxy carbonyl )piperidin-4-yl)thiazole-4-carboxylate

: 1192247-99-6
4-{4-[(cyclohexyloxy)carbonyl]-1,3-thiazol-2-yl}piperidinium chloride

Guidance literature:: Multi-step reaction with 3 steps

1: water; lithium hydroxide monohydrate / tetrahydrofuran / 4 h / 20 °C

2: dmap; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide / dichloromethane / 20 °C

3: hydrogenchloride / 1,4-dioxane; diethyl ether / 0 - 20 °C / Inert atmosphere

With hydrogenchloride; dmap; lithium hydroxide monohydrate; water; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In tetrahydrofuran; 1,4-dioxane; diethyl ether; dichloromethane;

Reference yield: 65.0%

: 922516-25-4
2-(3,5-bis(trifluoromethyl)-1H-pyrazol-1-yl)acetic acid

: 1192247-99-6
4-{4-[(cyclohexyloxy)carbonyl]-1,3-thiazol-2-yl}piperidinium chloride

: 1192761-73-1
cyclohexyl 2-(1-{[3,5-bis(trifluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazole-4-carboxylate

Guidance literature:: 2-(3,5-bis(trifluoromethyl)-1H-pyrazol-1-yl)acetic acid; With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 0.5h;

4-{4-[(cyclohexyloxy)carbonyl]-1,3-thiazol-2-yl}piperidinium chloride; With bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; In dichloromethane; at 20 ℃;