1-(4-(5-(4-isobutyl-5-phenylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)benzyl)-azetidine-3-carboxylic acid

Base Information

Chemical Name:1-(4-(5-(4-isobutyl-5-phenylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)benzyl)-azetidine-3-carboxylic acid
CAS No.:1236188-42-3
Molecular Formula:C₂₆H₂₆N₄O₄
Molecular Weight:458.517
Hs Code.:

Synonyms:1-(4-(5-(4-isobutyl-5-phenylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)benzyl)-azetidine-3-carboxylic acid

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Chemical Property of 1-(4-(5-(4-isobutyl-5-phenylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)benzyl)-azetidine-3-carboxylic acid

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Technology Process of 1-(4-(5-(4-isobutyl-5-phenylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)benzyl)-azetidine-3-carboxylic acid

There total 6 articles about 1-(4-(5-(4-isobutyl-5-phenylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)benzyl)-azetidine-3-carboxylic acid 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: 34.0%

: 1236188-95-6
tert-butyl 1-(4-(5-(4-isobutyl-5-phenylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)benzyl)azetidine-3-carboxylate

: 1236188-42-3
1-(4-(5-(4-isobutyl-5-phenylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)benzyl)-azetidine-3-carboxylic acid

Guidance literature:: With trifluoroacetic acid; for 0.5h;
DOI:10.1021/acs.jmedchem.6b00089

Reference yield:

: 105-07-7
4-cyanobenzaldehyde

: 1236188-42-3
1-(4-(5-(4-isobutyl-5-phenylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)benzyl)-azetidine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: sodium cyanoborohydride / methanol / 0 - 20 °C

2: hydroxylamine hydrochloride; sodium hydrogencarbonate / tert-butyl alcohol / 20 °C / Reflux

3: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 20 - 60 °C / Inert atmosphere

4: trifluoroacetic acid / 0.5 h

With hydroxylamine hydrochloride; sodium cyanoborohydride; sodium hydrogencarbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; In methanol; N,N-dimethyl-formamide; tert-butyl alcohol;
DOI:10.1021/acs.jmedchem.6b00089

Reference yield:

: 1236144-53-8
tert-butyl 1-(4-cyanobenzyl)azetidine-3-carboxylate

: 1236188-42-3
1-(4-(5-(4-isobutyl-5-phenylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)benzyl)-azetidine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: hydroxylamine hydrochloride; sodium hydrogencarbonate / tert-butyl alcohol / 20 °C / Reflux

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 20 - 60 °C / Inert atmosphere

3: trifluoroacetic acid / 0.5 h

With hydroxylamine hydrochloride; sodium hydrogencarbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; In N,N-dimethyl-formamide; tert-butyl alcohol;
DOI:10.1021/acs.jmedchem.6b00089