(S)-methyl 2-(4-bromophenyl)-3-((1-(tert-butoxycarbonyl)pyrrolidin-3-yl)methyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-1-ene-8-carboxylate

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Chemical Name:(S)-methyl 2-(4-bromophenyl)-3-((1-(tert-butoxycarbonyl)pyrrolidin-3-yl)methyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-1-ene-8-carboxylate
CAS No.:1579514-47-8
Molecular Formula:C₂₅H₃₃BrN₄O₅
Molecular Weight:549.465
Hs Code.:

Synonyms:(S)-methyl 2-(4-bromophenyl)-3-((1-(tert-butoxycarbonyl)pyrrolidin-3-yl)methyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-1-ene-8-carboxylate

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Chemical Property of (S)-methyl 2-(4-bromophenyl)-3-((1-(tert-butoxycarbonyl)pyrrolidin-3-yl)methyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-1-ene-8-carboxylate

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Technology Process of (S)-methyl 2-(4-bromophenyl)-3-((1-(tert-butoxycarbonyl)pyrrolidin-3-yl)methyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-1-ene-8-carboxylate

There total 6 articles about (S)-methyl 2-(4-bromophenyl)-3-((1-(tert-butoxycarbonyl)pyrrolidin-3-yl)methyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-1-ene-8-carboxylate 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: 81.0%

: 1067230-65-2
(R)-tert-butyl 3-(bromomethyl)pyrrolidine-1-carboxylate

: 1579514-45-6
methyl 2-(4-bromophenyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-1-ene-8-carboxylate

: 1579514-47-8
(S)-methyl 2-(4-bromophenyl)-3-((1-(tert-butoxycarbonyl)pyrrolidin-3-yl)methyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-1-ene-8-carboxylate

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 20 - 65 ℃; for 17h;

Reference yield:

: 288154-18-7
tert-butyl 4-amino-4-carbamoylpiperidine-1-carboxylate

: 1579514-47-8
(S)-methyl 2-(4-bromophenyl)-3-((1-(tert-butoxycarbonyl)pyrrolidin-3-yl)methyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-1-ene-8-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 24 h / 20 °C

2: sodium hydroxide / water; methanol / 24 h / 65 °C

3: hydrogenchloride / 1,4-dioxane / 5 h / 20 °C

4: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C

5: caesium carbonate / N,N-dimethyl-formamide / 17 h / 20 - 65 °C

With hydrogenchloride; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In 1,4-dioxane; methanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 1579514-39-8
4-tert-butyl 4-(4-bromobenzamido)-4-carbamoylpiperidine-1-carboxylate

: 1579514-47-8
(S)-methyl 2-(4-bromophenyl)-3-((1-(tert-butoxycarbonyl)pyrrolidin-3-yl)methyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-1-ene-8-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydroxide / water; methanol / 24 h / 65 °C

2: hydrogenchloride / 1,4-dioxane / 5 h / 20 °C

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C

4: caesium carbonate / N,N-dimethyl-formamide / 17 h / 20 - 65 °C

With hydrogenchloride; caesium carbonate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In 1,4-dioxane; methanol; dichloromethane; water; N,N-dimethyl-formamide;