(S)-tert-butyl 2-(4-(benzyloxy)phenyl)-1-(4-formyl-5-phenylthiazol-2-yl)ethylcarbamate

Base Information

Chemical Name:(S)-tert-butyl 2-(4-(benzyloxy)phenyl)-1-(4-formyl-5-phenylthiazol-2-yl)ethylcarbamate
CAS No.:1489278-67-2
Molecular Formula:C₃₀H₃₀N₂O₄S
Molecular Weight:514.645
Hs Code.:

Synonyms:(S)-tert-butyl 2-(4-(benzyloxy)phenyl)-1-(4-formyl-5-phenylthiazol-2-yl)ethylcarbamate

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Chemical Property of (S)-tert-butyl 2-(4-(benzyloxy)phenyl)-1-(4-formyl-5-phenylthiazol-2-yl)ethylcarbamate

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Technology Process of (S)-tert-butyl 2-(4-(benzyloxy)phenyl)-1-(4-formyl-5-phenylthiazol-2-yl)ethylcarbamate

There total 5 articles about (S)-tert-butyl 2-(4-(benzyloxy)phenyl)-1-(4-formyl-5-phenylthiazol-2-yl)ethylcarbamate 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:

: 1489278-51-4
C₃₀H₃₂N₂O₄S

: 1489278-67-2
(S)-tert-butyl 2-(4-(benzyloxy)phenyl)-1-(4-formyl-5-phenylthiazol-2-yl)ethylcarbamate

Guidance literature:: With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In dimethyl sulfoxide; toluene; at 50 ℃; for 2h;
DOI:10.1016/j.ejmech.2013.09.017

Reference yield:

: 2130-96-3,54784-43-9
O-benzyl-N-tert-butoxycarbonyl-L-tyrosine

: 1489278-67-2
(S)-tert-butyl 2-(4-(benzyloxy)phenyl)-1-(4-formyl-5-phenylthiazol-2-yl)ethylcarbamate

Guidance literature:: Multi-step reaction with 4 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap; triethylamine / dichloromethane / 2 h / 20 °C

2: Lawessons reagent / tetrahydrofuran / 2 h / 65 °C

3: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 - 20 °C

4: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / toluene; dimethyl sulfoxide / 2 h / 50 °C

With Lawessons reagent; dmap; lithium aluminium tetrahydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide; toluene;
DOI:10.1016/j.ejmech.2013.09.017

Reference yield:

: 95271-93-5
benzoylaminoacetic acid ethyl ester

: 1489278-67-2
(S)-tert-butyl 2-(4-(benzyloxy)phenyl)-1-(4-formyl-5-phenylthiazol-2-yl)ethylcarbamate

Guidance literature:: Multi-step reaction with 4 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap; triethylamine / dichloromethane / 2 h / 20 °C

2: Lawessons reagent / tetrahydrofuran / 2 h / 65 °C

3: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 - 20 °C

4: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / toluene; dimethyl sulfoxide / 2 h / 50 °C

With Lawessons reagent; dmap; lithium aluminium tetrahydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide; toluene;
DOI:10.1016/j.ejmech.2013.09.017