(R)-ethyl 2-[1-(tert-butoxycarbonylamino)-2-phenylethyl]thiazole-4-carboxylate

Base Information

Chemical Name:(R)-ethyl 2-[1-(tert-butoxycarbonylamino)-2-phenylethyl]thiazole-4-carboxylate
CAS No.:256384-34-6
Molecular Formula:C₁₉H₂₄N₂O₄S
Molecular Weight:376.477
Hs Code.:

Synonyms:(R)-ethyl 2-[1-(tert-butoxycarbonylamino)-2-phenylethyl]thiazole-4-carboxylate

Suppliers and Price of (R)-ethyl 2-[1-(tert-butoxycarbonylamino)-2-phenylethyl]thiazole-4-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 (R)-ethyl 2-[1-(tert-butoxycarbonylamino)-2-phenylethyl]thiazole-4-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-ethyl 2-[1-(tert-butoxycarbonylamino)-2-phenylethyl]thiazole-4-carboxylate

There total 8 articles about (R)-ethyl 2-[1-(tert-butoxycarbonylamino)-2-phenylethyl]thiazole-4-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:

: C₁₉H₂₆N₂O₅S

: 256384-34-6
(R)-ethyl 2-[1-(tert-butoxycarbonylamino)-2-phenylethyl]thiazole-4-carboxylate

Guidance literature:: C₁₉H₂₆N₂O₅S; With pyridine; trifluoroacetic anhydride; In 1,2-dimethoxyethane; at 0 ℃; for 2h; Inert atmosphere;

With triethylamine; In 1,2-dimethoxyethane; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.1016/j.tetlet.2014.10.089

Reference yield:

: 129095-62-1,35150-06-2
(R)-tert-butyl (1-amino-1-oxo-3-phenylpropan-2-yl)carbamate

: 256384-34-6
(R)-ethyl 2-[1-(tert-butoxycarbonylamino)-2-phenylethyl]thiazole-4-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: Lawessons reagent / dichloromethane / 12 h / 20 °C

2: potassium hydrogencarbonate / 1,2-dimethoxyethane / -40 - -20 °C / Inert atmosphere

3: 2,6-dimethylpyridine; trifluoroacetic anhydride / 1,2-dimethoxyethane / -40 - -20 °C / Inert atmosphere

With Lawessons reagent; 2,6-dimethylpyridine; potassium hydrogencarbonate; trifluoroacetic anhydride; In 1,2-dimethoxyethane; dichloromethane;
DOI:10.1021/jo201675r

Reference yield:

: 18942-49-9
Boc-D-Phe-OH

: 256384-34-6
(R)-ethyl 2-[1-(tert-butoxycarbonylamino)-2-phenylethyl]thiazole-4-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / dichloromethane / 0.33 h / 20 °C

1.2: 2 h / 20 °C

2.1: Lawessons reagent / dichloromethane / 12 h / 20 °C

3.1: potassium hydrogencarbonate / 1,2-dimethoxyethane / -40 - -20 °C / Inert atmosphere

4.1: 2,6-dimethylpyridine; trifluoroacetic anhydride / 1,2-dimethoxyethane / -40 - -20 °C / Inert atmosphere

With Lawessons reagent; 2,6-dimethylpyridine; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; potassium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; trifluoroacetic anhydride; In 1,2-dimethoxyethane; dichloromethane;
DOI:10.1021/jo201675r