benzyl <<<(tert-butoxycarbonyl)phenyl>carbamoyl>methyl>carbamate

Base Information

• Chemical Name: benzyl <<<(tert-butoxycarbonyl)phenyl>carbamoyl>methyl>carbamate
• CAS No.: 106880-81-3
• Molecular Formula: C₂₁H₂₄N₂O₅
• Molecular Weight: 384.432
• Mol file: 106880-81-3.mol

Synonyms:benzyl <<<(tert-butoxycarbonyl)phenyl>carbamoyl>methyl>carbamate

Chemical Property of benzyl <<<(tert-butoxycarbonyl)phenyl>carbamoyl>methyl>carbamate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of benzyl <<<(tert-butoxycarbonyl)phenyl>carbamoyl>methyl>carbamate

There total 3 articles about benzyl <<<(tert-butoxycarbonyl)phenyl>carbamoyl>methyl>carbamate 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: 80.0%

tert-butyl 2-aminobenzoate (64113-91-3) + N-(Benzyloxycarbonyl)glycine (1138-80-3) → benzyl <<<(tert-butoxycarbonyl)phenyl>carbamoyl>methyl>carbamate (106880-81-3)

Guidance literature:

With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; for 168h; Ambient temperature;

DOI:10.1021/ja00240a036

Reference yield:

N-(trifluoroacetyl)anthranilic acid (19165-29-8) → benzyl <<<(tert-butoxycarbonyl)phenyl>carbamoyl>methyl>carbamate (106880-81-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) N,N'-carbonylbisimidazole / 1.) 2 h, RT; 2.) tert-butyl alcohol, 36 h, RT, and ethanol, sodium borohydride, 0 deg C, ca. 25 min

2: 80 percent / N-ethyl-N'-((dimethylamino)propyl)carbodiimide hydrochloride / CH₂Cl₂ / 168 h / Ambient temperature

With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 1,1'-carbonyldiimidazole; In dichloromethane;

DOI:10.1021/ja00240a036

Reference yield:

anthranilic acid (118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4) → benzyl <<<(tert-butoxycarbonyl)phenyl>carbamoyl>methyl>carbamate (106880-81-3)

Guidance literature:

Multi-step reaction with 3 steps

1: 81 percent

2: 1.) N,N'-carbonylbisimidazole / 1.) 2 h, RT; 2.) tert-butyl alcohol, 36 h, RT, and ethanol, sodium borohydride, 0 deg C, ca. 25 min

3: 80 percent / N-ethyl-N'-((dimethylamino)propyl)carbodiimide hydrochloride / CH₂Cl₂ / 168 h / Ambient temperature

With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 1,1'-carbonyldiimidazole; In dichloromethane;

DOI:10.1021/ja00240a036

upstream raw materials:

tert-butyl 2-aminobenzoate

N-(Benzyloxycarbonyl)glycine

N-(trifluoroacetyl)anthranilic acid

anthranilic acid

Downstream raw materials:

tert-butyl N-glycylanthranilate hydrochloride