9-ethyl-8-(2-methylpyrimidin-5-yl)-N-[(3S)-1-(phenylacetyl)pyrrolidin-3-yl]-9H-purin-6-amine

Base Information

Chemical Name:9-ethyl-8-(2-methylpyrimidin-5-yl)-N-[(3S)-1-(phenylacetyl)pyrrolidin-3-yl]-9H-purin-6-amine
CAS No.:1610703-98-4
Molecular Formula:C₂₄H₂₆N₈O
Molecular Weight:442.523
Hs Code.:

Synonyms:9-ethyl-8-(2-methylpyrimidin-5-yl)-N-[(3S)-1-(phenylacetyl)pyrrolidin-3-yl]-9H-purin-6-amine

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Chemical Property of 9-ethyl-8-(2-methylpyrimidin-5-yl)-N-[(3S)-1-(phenylacetyl)pyrrolidin-3-yl]-9H-purin-6-amine

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Technology Process of 9-ethyl-8-(2-methylpyrimidin-5-yl)-N-[(3S)-1-(phenylacetyl)pyrrolidin-3-yl]-9H-purin-6-amine

There total 6 articles about 9-ethyl-8-(2-methylpyrimidin-5-yl)-N-[(3S)-1-(phenylacetyl)pyrrolidin-3-yl]-9H-purin-6-amine 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:

: 103-82-2
phenylacetic acid

: (S)-9-ethyl-8-(2-methylpyrimidin-5-yl)-N-(pyrrolidin-3-yl)-9H-purin-6-amine dihydrochloride

: 1610703-98-4
9-ethyl-8-(2-methylpyrimidin-5-yl)-N-[(3S)-1-(phenylacetyl)pyrrolidin-3-yl]-9H-purin-6-amine

Guidance literature:: phenylacetic acid; (S)-9-ethyl-8-(2-methylpyrimidin-5-yl)-N-(pyrrolidin-3-yl)-9H-purin-6-amine dihydrochloride; With 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium-3-oxid hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 16h;

With trifluoroacetic acid; In water; acetonitrile;

Reference yield:

: 98140-03-5
6-chloro-N⁴-ethylpyrimidine-4,5-diamine

: 1610703-98-4
9-ethyl-8-(2-methylpyrimidin-5-yl)-N-[(3S)-1-(phenylacetyl)pyrrolidin-3-yl]-9H-purin-6-amine

Guidance literature:: Multi-step reaction with 5 steps

1: sodium t-butanolate / Dimethyl ether / 2 h / 20 - 43 °C

2: N,O-bis-(trimethylsilyl)-acetamide / 1 h / 55 °C

3: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 48 h / 60 °C

4: hydrogenchloride / 1,4-dioxane / 16 h

5: N-ethyl-N,N-diisopropylamine; 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium-3-oxid hexafluorophosphate / N,N-dimethyl-formamide / 16 h / 20 °C

With hydrogenchloride; N,O-bis-(trimethylsilyl)-acetamide; 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium-3-oxid hexafluorophosphate; N-ethyl-N,N-diisopropylamine; sodium t-butanolate; In 1,4-dioxane; Dimethyl ether; N,N-dimethyl-formamide;

Reference yield:

: 2134-38-5
ethyl 2-methylpyrimidine-5-carboxylate

: 1610703-98-4
9-ethyl-8-(2-methylpyrimidin-5-yl)-N-[(3S)-1-(phenylacetyl)pyrrolidin-3-yl]-9H-purin-6-amine

Guidance literature:: Multi-step reaction with 5 steps

1: sodium t-butanolate / Dimethyl ether / 2 h / 20 - 43 °C

2: N,O-bis-(trimethylsilyl)-acetamide / 1 h / 55 °C

3: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 48 h / 60 °C

4: hydrogenchloride / 1,4-dioxane / 16 h

5: N-ethyl-N,N-diisopropylamine; 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium-3-oxid hexafluorophosphate / N,N-dimethyl-formamide / 16 h / 20 °C

With hydrogenchloride; N,O-bis-(trimethylsilyl)-acetamide; 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium-3-oxid hexafluorophosphate; N-ethyl-N,N-diisopropylamine; sodium t-butanolate; In 1,4-dioxane; Dimethyl ether; N,N-dimethyl-formamide;