(S)-1-{(S)-2-[(S)-2-(tert-butoxycarbonylmethylamino)propionylamino]-2-phenylacetyl}-2,3-dihydro-1H-indole-2-carboxylic acid

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Chemical Name:(S)-1-{(S)-2-[(S)-2-(tert-butoxycarbonylmethylamino)propionylamino]-2-phenylacetyl}-2,3-dihydro-1H-indole-2-carboxylic acid
CAS No.:1599453-98-1
Molecular Formula:C₂₆H₃₁N₃O₆
Molecular Weight:481.549
Hs Code.:

Synonyms:(S)-1-{(S)-2-[(S)-2-(tert-butoxycarbonylmethylamino)propionylamino]-2-phenylacetyl}-2,3-dihydro-1H-indole-2-carboxylic acid

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Chemical Property of (S)-1-{(S)-2-[(S)-2-(tert-butoxycarbonylmethylamino)propionylamino]-2-phenylacetyl}-2,3-dihydro-1H-indole-2-carboxylic acid

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Technology Process of (S)-1-{(S)-2-[(S)-2-(tert-butoxycarbonylmethylamino)propionylamino]-2-phenylacetyl}-2,3-dihydro-1H-indole-2-carboxylic acid

There total 5 articles about (S)-1-{(S)-2-[(S)-2-(tert-butoxycarbonylmethylamino)propionylamino]-2-phenylacetyl}-2,3-dihydro-1H-indole-2-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:

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

: 1599453-98-1
(S)-1-{(S)-2-[(S)-2-(tert-butoxycarbonylmethylamino)propionylamino]-2-phenylacetyl}-2,3-dihydro-1H-indole-2-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1: pyridine; trifluoro-[1,3,5]triazine / dichloromethane / 2 h / 23 °C

2: 2,6-di-tert-butyl-pyridine / dichloromethane / 20 °C

3: hydrogenchloride / water; 1,4-dioxane / 2 h / 20 °C

4: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / dichloromethane / 20 °C

5: lithium hydroxide; methanol / tetrahydrofuran; water / 2.5 h / 23 °C

With pyridine; hydrogenchloride; methanol; trifluoro-[1,3,5]triazine; 2,6-di-tert-butyl-pyridine; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water;

Reference yield:

: 1599453-97-0
(S)-1-{(S)-2-[(S)-2-(tert-butoxycarbonylmethylamino)propionylamino]-2-phenylacetyl}-2,3-dihydro-1H-indole-2-carboxylic acid ethyl ester

: 1599453-98-1
(S)-1-{(S)-2-[(S)-2-(tert-butoxycarbonylmethylamino)propionylamino]-2-phenylacetyl}-2,3-dihydro-1H-indole-2-carboxylic acid

Guidance literature:: With methanol; lithium hydroxide; In tetrahydrofuran; water; at 23 ℃; for 2.5h;

Reference yield:

: 1599453-96-9
(S)-1-((S)-2-amino-2-phenylacetyl)-2,3-dihydro-1H-indole-2-carboxylic acid ethyl ester hydrochloride

: 1599453-98-1
(S)-1-{(S)-2-[(S)-2-(tert-butoxycarbonylmethylamino)propionylamino]-2-phenylacetyl}-2,3-dihydro-1H-indole-2-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / dichloromethane / 20 °C

2: lithium hydroxide; methanol / tetrahydrofuran; water / 2.5 h / 23 °C

With methanol; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; lithium hydroxide; In tetrahydrofuran; dichloromethane; water;