(2,4-diphenyl-oxazol-5-yl)-(2-propyl-pentanoyl)-carbamic acid tert-butyl ester

Base Information

Chemical Name:(2,4-diphenyl-oxazol-5-yl)-(2-propyl-pentanoyl)-carbamic acid tert-butyl ester
CAS No.:1026925-54-1
Molecular Formula:C₂₈H₃₄N₂O₄
Molecular Weight:462.589
Hs Code.:

(2,4-diphenyl-oxazol-5-yl)-(2-propyl-pentanoyl)-carbamic acid <i>tert</i>-butyl ester

Synonyms:(2,4-diphenyl-oxazol-5-yl)-(2-propyl-pentanoyl)-carbamic acid tert-butyl ester

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Chemical Property of (2,4-diphenyl-oxazol-5-yl)-(2-propyl-pentanoyl)-carbamic acid tert-butyl ester

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Technology Process of (2,4-diphenyl-oxazol-5-yl)-(2-propyl-pentanoyl)-carbamic acid tert-butyl ester

There total 4 articles about (2,4-diphenyl-oxazol-5-yl)-(2-propyl-pentanoyl)-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:

: 934235-75-3
tert-butyl 2,4-diphenyloxazol-5-ylcarbamate

: 2936-08-5
valproyl chloride

: 1026925-54-1
(2,4-diphenyl-oxazol-5-yl)-(2-propyl-pentanoyl)-carbamic acid tert-butyl ester

Guidance literature:: With dmap; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 2.5h;
DOI:10.1021/jm0612719

Reference yield:

: C₁₆H₁₁ClN₂O₂

: 1026925-54-1
(2,4-diphenyl-oxazol-5-yl)-(2-propyl-pentanoyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.07 g / CH₂Cl₂ / 0.08 h / 20 °C

2: N,N-diisopropylethylamine; DMAP / CH₂Cl₂ / 2.5 h / 20 °C

With dmap; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1021/jm0612719

Reference yield:

: 99-66-1
valproic acid

: 1026925-54-1
(2,4-diphenyl-oxazol-5-yl)-(2-propyl-pentanoyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: oxalyl chloride; DMF / CH₂Cl₂ / 1 h

2: N,N-diisopropylethylamine; DMAP / CH₂Cl₂ / 2.5 h / 20 °C

With dmap; oxalyl dichloride; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; In dichloromethane;
DOI:10.1021/jm0612719