tert-butyl 4-({3-[(R)-cyclohexyl(hydroxy)phenylmethy]-1H-1,2,4-triazol-1-yl}methyl)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-({3-[(R)-cyclohexyl(hydroxy)phenylmethy]-1H-1,2,4-triazol-1-yl}methyl)piperidine-1-carboxylate
CAS No.:1204122-42-8
Molecular Formula:C₂₆H₃₈N₄O₃
Molecular Weight:454.613
Hs Code.:

Synonyms:tert-butyl 4-({3-[(R)-cyclohexyl(hydroxy)phenylmethy]-1H-1,2,4-triazol-1-yl}methyl)piperidine-1-carboxylate

Suppliers and Price of tert-butyl 4-({3-[(R)-cyclohexyl(hydroxy)phenylmethy]-1H-1,2,4-triazol-1-yl}methyl)piperidine-1-carboxylate

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 tert-butyl 4-({3-[(R)-cyclohexyl(hydroxy)phenylmethy]-1H-1,2,4-triazol-1-yl}methyl)piperidine-1-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tert-butyl 4-({3-[(R)-cyclohexyl(hydroxy)phenylmethy]-1H-1,2,4-triazol-1-yl}methyl)piperidine-1-carboxylate

There total 5 articles about tert-butyl 4-({3-[(R)-cyclohexyl(hydroxy)phenylmethy]-1H-1,2,4-triazol-1-yl}methyl)piperidine-1-carboxylate 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: 64.0%

: 1204122-40-6
(R)-cyclohexyl(phenyl)1H-1,2,4-triazol-3-ylmethanol

: 158407-04-6
tert-butyl 4-(bromomethyl)piperidine-1-carboxylate

: 1204122-42-8
tert-butyl 4-({3-[(R)-cyclohexyl(hydroxy)phenylmethy]-1H-1,2,4-triazol-1-yl}methyl)piperidine-1-carboxylate

Guidance literature:: With caesium carbonate; In acetone; at 20 - 70 ℃; Product distribution / selectivity;

Reference yield:

: 1204122-37-1
(2R)-2-cyclohexyl-2-hydroxy-2-phenylacetamide

: 1204122-42-8
tert-butyl 4-({3-[(R)-cyclohexyl(hydroxy)phenylmethy]-1H-1,2,4-triazol-1-yl}methyl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: toluene / 2 h / 90 °C

2: hydrazine hydrate; acetic acid / toluene / 2 h / 90 °C

3: caesium carbonate / acetone / 5 h / 70 °C

With caesium carbonate; hydrazine hydrate; acetic acid; In acetone; toluene;
DOI:10.1016/j.bmcl.2015.10.008

Reference yield:

: 4335-77-7,20585-34-6,20585-39-1,50896-04-3
cyclohexylmandelic acid

: 1204122-42-8
tert-butyl 4-({3-[(R)-cyclohexyl(hydroxy)phenylmethy]-1H-1,2,4-triazol-1-yl}methyl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: D-tyrosine methyl ester / water; acetonitrile / 80 °C

2: ammonia; 1,1'-carbonyldiimidazole / toluene / 24 h / 20 °C

3: toluene / 2 h / 90 °C

4: hydrazine hydrate; acetic acid / toluene / 2 h / 90 °C

5: caesium carbonate / acetone / 5 h / 70 °C

With D-tyrosine methyl ester; ammonia; caesium carbonate; hydrazine hydrate; acetic acid; 1,1'-carbonyldiimidazole; In water; acetone; toluene; acetonitrile;
DOI:10.1016/j.bmcl.2015.10.008