{4-[5-(5-tert-butyl-oxazol-2-ylmethylsulfanyl)-thiazol-2-ylcarbamoyl]-cyclohexyl}-carbamic acid tert-butyl ester

Base Information

• Chemical Name: {4-[5-(5-tert-butyl-oxazol-2-ylmethylsulfanyl)-thiazol-2-ylcarbamoyl]-cyclohexyl}-carbamic acid tert-butyl ester
• CAS No.: 371114-60-2
• Molecular Formula: C₂₃H₃₄N₄O₄S₂
• Molecular Weight: 494.679
• Mol file: 371114-60-2.mol

Synonyms:{4-[5-(5-tert-butyl-oxazol-2-ylmethylsulfanyl)-thiazol-2-ylcarbamoyl]-cyclohexyl}-carbamic acid tert-butyl ester

Chemical Property of {4-[5-(5-tert-butyl-oxazol-2-ylmethylsulfanyl)-thiazol-2-ylcarbamoyl]-cyclohexyl}-carbamic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of {4-[5-(5-tert-butyl-oxazol-2-ylmethylsulfanyl)-thiazol-2-ylcarbamoyl]-cyclohexyl}-carbamic acid tert-butyl ester

There total 8 articles about {4-[5-(5-tert-butyl-oxazol-2-ylmethylsulfanyl)-thiazol-2-ylcarbamoyl]-cyclohexyl}-carbamic acid tert-butyl 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: 43.0%

trans-4-(tert-butoxycarbonylamino)cyclohexane carboxylic acid (130309-46-5) + 2-amino-5-[[[5-(1,1-dimethylethyl)-2-oxazolyl]methyl]thio]-thiazole (224436-97-9) → {4-[5-(5-tert-butyl-oxazol-2-ylmethylsulfanyl)-thiazol-2-ylcarbamoyl]-cyclohexyl}-carbamic acid tert-butyl ester (371114-60-2)

Guidance literature:

With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃;

DOI:10.1021/jm0305568

Reference yield:

1-azido-3,3-dimethyl-2-butanone (76779-98-1) → {4-[5-(5-tert-butyl-oxazol-2-ylmethylsulfanyl)-thiazol-2-ylcarbamoyl]-cyclohexyl}-carbamic acid tert-butyl ester (371114-60-2)

Guidance literature:

Multi-step reaction with 5 steps

1.1: 28.0 g / aq. HCl; H₂ / Pd/C / methanol / 2 h / 1034.3 Torr

2.1: 98 percent / Et₃N / CH₂Cl₂ / 1 h / -10 °C

3.1: 80 percent / POCl₃ / 1 h / 105 °C

4.1: NaBH₄ / ethanol / 1 h / 20 °C

4.2: 94 percent / ethanol; acetone / 1 h / Heating

5.1: 43 percent / 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride / dimethylformamide; CH₂Cl₂ / 20 °C

With hydrogenchloride; sodium tetrahydroborate; hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trichlorophosphate; palladium on activated charcoal; In methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1021/jm0305568

Reference yield:

1-Bromopinacolon (5469-26-1) → {4-[5-(5-tert-butyl-oxazol-2-ylmethylsulfanyl)-thiazol-2-ylcarbamoyl]-cyclohexyl}-carbamic acid tert-butyl ester (371114-60-2)

Guidance literature:

Multi-step reaction with 6 steps

1.1: NaN₃ / acetone / 20 °C

2.1: 28.0 g / aq. HCl; H₂ / Pd/C / methanol / 2 h / 1034.3 Torr

3.1: 98 percent / Et₃N / CH₂Cl₂ / 1 h / -10 °C

4.1: 80 percent / POCl₃ / 1 h / 105 °C

5.1: NaBH₄ / ethanol / 1 h / 20 °C

5.2: 94 percent / ethanol; acetone / 1 h / Heating

6.1: 43 percent / 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride / dimethylformamide; CH₂Cl₂ / 20 °C

With hydrogenchloride; sodium tetrahydroborate; sodium azide; hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trichlorophosphate; palladium on activated charcoal; In methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; acetone;

DOI:10.1021/jm0305568

upstream raw materials:

trans-4-(tert-butoxycarbonylamino)cyclohexane carboxylic acid

2-amino-5-[[[5-(1,1-dimethylethyl)-2-oxazolyl]methyl]thio]-thiazole

4-aminocyclohexanecarboxylic acid

1-azido-3,3-dimethyl-2-butanone