2-(1-tert-butoxycarbonylamino-3-methoxycarbonyl-propyl)-thiazole-4-carboxylic acid benzyl ester

Base Information

Chemical Name:2-(1-tert-butoxycarbonylamino-3-methoxycarbonyl-propyl)-thiazole-4-carboxylic acid benzyl ester
CAS No.:347894-95-5
Molecular Formula:C₂₁H₂₆N₂O₆S
Molecular Weight:434.513
Hs Code.:

2-(1-<i>tert</i>-butoxycarbonylamino-3-methoxycarbonyl-propyl)-thiazole-4-carboxylic acid benzyl ester

Synonyms:2-(1-tert-butoxycarbonylamino-3-methoxycarbonyl-propyl)-thiazole-4-carboxylic acid benzyl ester

Suppliers and Price of 2-(1-tert-butoxycarbonylamino-3-methoxycarbonyl-propyl)-thiazole-4-carboxylic acid benzyl ester

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 2-(1-tert-butoxycarbonylamino-3-methoxycarbonyl-propyl)-thiazole-4-carboxylic acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-(1-tert-butoxycarbonylamino-3-methoxycarbonyl-propyl)-thiazole-4-carboxylic acid benzyl ester

There total 13 articles about 2-(1-tert-butoxycarbonylamino-3-methoxycarbonyl-propyl)-thiazole-4-carboxylic acid benzyl ester 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: 73.0%

: C₂₁H₃₀N₂O₇S

: 347894-95-5
2-(1-tert-butoxycarbonylamino-3-methoxycarbonyl-propyl)-thiazole-4-carboxylic acid benzyl ester

Guidance literature:: C₂₁H₃₀N₂O₇S; With diethylamino-sulfur trifluoride; In dichloromethane; at -78 - 20 ℃; Inert atmosphere;

With Bromotrichloromethane; In dichloromethane; at 0 ℃; for 0.166667h; Inert atmosphere;

With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/ja203894r

Reference yield:

: 2-(1-tert-butoxycarbonylamino-3-methoxycarbonyl-propyl)-4,5-dihydro-thiazole-4-carboxylic acid benzyl ester

: 347894-95-5
2-(1-tert-butoxycarbonylamino-3-methoxycarbonyl-propyl)-thiazole-4-carboxylic acid benzyl ester

Guidance literature:: With Bromotrichloromethane; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 0 ℃; for 4h;
DOI:10.1039/b101417j

Reference yield:

: 45214-91-3
(2S)-2-[(tert-butoxy)carbonylamino]-4-(methoxycarbonyl)butanoic acid

: 347894-95-5
2-(1-tert-butoxycarbonylamino-3-methoxycarbonyl-propyl)-thiazole-4-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: HOBt; EDCI*HCl; NMM / CH₂Cl₂ / 0.5 h / 0 °C

1.2: 94 percent / NMM / CH₂Cl₂ / 48 h / 0 - 20 °C

2.1: 86 percent / Et₃N; DMAP / CH₂Cl₂ / 14 h

3.1: 94 percent / Lawesson's reagent / benzene / 14 h / 80 °C

4.1: 91 percent / TBAF / tetrahydrofuran / 3 h / 0 °C

5.1: Burgess' reagent / tetrahydrofuran / 0.5 h / 65 °C

6.1: CBrCl₃; DBU / CH₂Cl₂ / 4 h / 0 °C

With Lawessons reagent; 4-methyl-morpholine; dmap; Burgess Reagent; Bromotrichloromethane; tetrabutyl ammonium fluoride; benzotriazol-1-ol; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; dichloromethane; benzene;
DOI:10.1039/b101417j