3-(4-(2-(5-((5-tert-butyloxazol-2-yl)methylthio)-thiazol-2-ylamino)-2-oxoethyl)phenoxy)-N-hydroxypropanamide

Base Information

Chemical Name:3-(4-(2-(5-((5-tert-butyloxazol-2-yl)methylthio)-thiazol-2-ylamino)-2-oxoethyl)phenoxy)-N-hydroxypropanamide
CAS No.:1133000-85-7
Molecular Formula:C₂₂H₂₆N₄O₅S₂
Molecular Weight:490.604
Hs Code.:

Synonyms:3-(4-(2-(5-((5-tert-butyloxazol-2-yl)methylthio)-thiazol-2-ylamino)-2-oxoethyl)phenoxy)-N-hydroxypropanamide

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Chemical Property of 3-(4-(2-(5-((5-tert-butyloxazol-2-yl)methylthio)-thiazol-2-ylamino)-2-oxoethyl)phenoxy)-N-hydroxypropanamide

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Technology Process of 3-(4-(2-(5-((5-tert-butyloxazol-2-yl)methylthio)-thiazol-2-ylamino)-2-oxoethyl)phenoxy)-N-hydroxypropanamide

There total 7 articles about 3-(4-(2-(5-((5-tert-butyloxazol-2-yl)methylthio)-thiazol-2-ylamino)-2-oxoethyl)phenoxy)-N-hydroxypropanamide 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%

: 1133000-87-9
methyl 3-(4-(2-(5-((5-tert-butyloxazol-2-yl)methylthio)thiazol-2-ylamino)-2-oxoethyl)phenoxy)propanoate

: 1133000-85-7
3-(4-(2-(5-((5-tert-butyloxazol-2-yl)methylthio)-thiazol-2-ylamino)-2-oxoethyl)phenoxy)-N-hydroxypropanamide

Guidance literature:: With hydroxylamine; In methanol; at 20 ℃; for 1h;

Reference yield:

: 13547-70-1
1-chloro-3,3-dimethyl-butan-2-one

: 1133000-85-7
3-(4-(2-(5-((5-tert-butyloxazol-2-yl)methylthio)-thiazol-2-ylamino)-2-oxoethyl)phenoxy)-N-hydroxypropanamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium azide / acetone / 25 °C

2.1: hydrogenchloride; hydrogen / palladium 10% on activated carbon / methanol

3.1: triethylamine / dichloromethane / 1.25 h / -10 - -5 °C

4.1: trichlorophosphate / 1 h / 105 °C

5.1: ethanol; sodium tetrahydroborate / acetone / 1 h / 20 °C

5.2: 1 h / Reflux

6.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 20 - 30 °C

7.1: hydroxylamine / methanol / 1 h / 20 °C

With hydrogenchloride; sodium tetrahydroborate; sodium azide; ethanol; hydrogen; hydroxylamine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trichlorophosphate; palladium 10% on activated carbon; In methanol; dichloromethane; N,N-dimethyl-formamide; acetone;

Reference yield:

: 76779-98-1
1-azido-3,3-dimethyl-2-butanone

: 1133000-85-7
3-(4-(2-(5-((5-tert-butyloxazol-2-yl)methylthio)-thiazol-2-ylamino)-2-oxoethyl)phenoxy)-N-hydroxypropanamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: hydrogenchloride; hydrogen / palladium 10% on activated carbon / methanol

2.1: triethylamine / dichloromethane / 1.25 h / -10 - -5 °C

3.1: trichlorophosphate / 1 h / 105 °C

4.1: ethanol; sodium tetrahydroborate / acetone / 1 h / 20 °C

4.2: 1 h / Reflux

5.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 20 - 30 °C

6.1: hydroxylamine / methanol / 1 h / 20 °C

With hydrogenchloride; sodium tetrahydroborate; ethanol; hydrogen; hydroxylamine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trichlorophosphate; palladium 10% on activated carbon; In methanol; dichloromethane; N,N-dimethyl-formamide; acetone;