(S)-2-tert-butyloxycarbonylamino-4-(1-benzyloxycarbonylpiperidin-4-yl)butanoic acid

Base Information

Chemical Name:(S)-2-tert-butyloxycarbonylamino-4-(1-benzyloxycarbonylpiperidin-4-yl)butanoic acid
CAS No.:1322746-29-1
Molecular Formula:C₂₂H₃₂N₂O₆
Molecular Weight:420.506
Hs Code.:

Synonyms:(S)-2-tert-butyloxycarbonylamino-4-(1-benzyloxycarbonylpiperidin-4-yl)butanoic acid

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Chemical Property of (S)-2-tert-butyloxycarbonylamino-4-(1-benzyloxycarbonylpiperidin-4-yl)butanoic acid

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Technology Process of (S)-2-tert-butyloxycarbonylamino-4-(1-benzyloxycarbonylpiperidin-4-yl)butanoic acid

There total 4 articles about (S)-2-tert-butyloxycarbonylamino-4-(1-benzyloxycarbonylpiperidin-4-yl)butanoic 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: 97.0%

: 1322746-28-0
(S)-2-tert-butyloxycarbonylamino-4-(1-benzyloxycarbonylpiperidin-4-yl)butanoic acid methyl ester

: 1322746-29-1
(S)-2-tert-butyloxycarbonylamino-4-(1-benzyloxycarbonylpiperidin-4-yl)butanoic acid

Guidance literature:: (S)-2-tert-butyloxycarbonylamino-4-(1-benzyloxycarbonylpiperidin-4-yl)butanoic acid methyl ester; With lithium hydroxide; In 1,4-dioxane; water; at 20 ℃; for 2h;

With hydrogenchloride; In 1,4-dioxane; water;

Reference yield:

: 121056-95-9,89524-98-1
trimethyl 2-(tert-butoxycarbonylamino)phosphonoacetate

: 1322746-29-1
(S)-2-tert-butyloxycarbonylamino-4-(1-benzyloxycarbonylpiperidin-4-yl)butanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: N,N,N',N'-tetramethylguanidine / tetrahydrofuran / 0.33 h / -78 °C

1.2: -78 - 0 °C

2.1: hydrogen / (+)-1,2-bis-((2S,5S)-2,5-diethylphospholano)benzene(cyclooctadiene)rhodium(I) trifluoromethanesulfonate / methanol / 18.5 h / 20 °C / 3000.3 Torr / Inert atmosphere

3.1: lithium hydroxide / 1,4-dioxane; water / 2 h / 20 °C

With hydrogen; lithium hydroxide; N,N,N',N'-tetramethylguanidine; (+)-1,2-bis-((2S,5S)-2,5-diethylphospholano)benzene(cyclooctadiene)rhodium(I) trifluoromethanesulfonate; In tetrahydrofuran; 1,4-dioxane; methanol; water;

Reference yield:

: 130312-10-6
benzyl 4-(2-oxoethyl)piperidine-1-carboxylate

: 1322746-29-1
(S)-2-tert-butyloxycarbonylamino-4-(1-benzyloxycarbonylpiperidin-4-yl)butanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: N,N,N',N'-tetramethylguanidine / tetrahydrofuran / 0.33 h / -78 °C

1.2: -78 - 0 °C

2.1: hydrogen / (+)-1,2-bis-((2S,5S)-2,5-diethylphospholano)benzene(cyclooctadiene)rhodium(I) trifluoromethanesulfonate / methanol / 18.5 h / 20 °C / 3000.3 Torr / Inert atmosphere

3.1: lithium hydroxide / 1,4-dioxane; water / 2 h / 20 °C

With hydrogen; lithium hydroxide; N,N,N',N'-tetramethylguanidine; (+)-1,2-bis-((2S,5S)-2,5-diethylphospholano)benzene(cyclooctadiene)rhodium(I) trifluoromethanesulfonate; In tetrahydrofuran; 1,4-dioxane; methanol; water;