(S)-4-(2-(4-(tert-butyl)phenylsulfonamido)-2-phenylacetamido)-Nhydroxybenzamide

Base Information

Chemical Name:(S)-4-(2-(4-(tert-butyl)phenylsulfonamido)-2-phenylacetamido)-Nhydroxybenzamide
CAS No.:1446014-67-0
Molecular Formula:C₂₅H₂₇N₃O₅S
Molecular Weight:481.572
Hs Code.:

Synonyms:(S)-4-(2-(4-(tert-butyl)phenylsulfonamido)-2-phenylacetamido)-Nhydroxybenzamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (S)-4-(2-(4-(tert-butyl)phenylsulfonamido)-2-phenylacetamido)-Nhydroxybenzamide

Chemical Property:

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Technology Process of (S)-4-(2-(4-(tert-butyl)phenylsulfonamido)-2-phenylacetamido)-Nhydroxybenzamide

There total 7 articles about (S)-4-(2-(4-(tert-butyl)phenylsulfonamido)-2-phenylacetamido)-Nhydroxybenzamide 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: 48.0%

: 1587675-61-3
(S)-methyl 4-(2-(4-(tert-butyl)phenylsulfonamido)-2-phenylacetamido)benzoate

: 1446014-67-0
(S)-4-(2-(4-(tert-butyl)phenylsulfonamido)-2-phenylacetamido)-Nhydroxybenzamide

Guidance literature:: With hydroxylamine potassium salt; In methanol; at 20 ℃; for 2h;
DOI:10.1002/cmdc.201300297

Reference yield:

: 2900-27-8
(2S)-2-[(tert-butoxycarbonyl)amino]-2-phenylethanoic acid

: 1446014-67-0
(S)-4-(2-(4-(tert-butyl)phenylsulfonamido)-2-phenylacetamido)-Nhydroxybenzamide

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / tetrahydrofuran / 8 h / 25 °C

2: ethyl acetate; hydrogenchloride / 5 h / 25 °C

3: sodium hydrogencarbonate / water; tetrahydrofuran / 8 h / 20 °C

4: hydroxylamine potassium salt / methanol / 2 h / 20 °C

With hydrogenchloride; hydroxylamine potassium salt; sodium hydrogencarbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; ethyl acetate; triethylamine; In tetrahydrofuran; methanol; water;
DOI:10.1002/cmdc.201300297

Reference yield:

: 2935-35-5
(S)-2-phenylglycine

: 1446014-67-0
(S)-4-(2-(4-(tert-butyl)phenylsulfonamido)-2-phenylacetamido)-Nhydroxybenzamide

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / methanol; water / 8 h / 25 °C

2: triethylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / tetrahydrofuran / 8 h / 25 °C

3: ethyl acetate; hydrogenchloride / 5 h / 25 °C

4: sodium hydrogencarbonate / water; tetrahydrofuran / 8 h / 20 °C

5: hydroxylamine potassium salt / methanol / 2 h / 20 °C

With hydrogenchloride; hydroxylamine potassium salt; sodium hydrogencarbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; ethyl acetate; triethylamine; In tetrahydrofuran; methanol; water;
DOI:10.1002/cmdc.201300297