2-(3-chloro-5-fluorophenylamino)-6-(7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)hexahydroindolizin-3(5H)-one

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Chemical Name:2-(3-chloro-5-fluorophenylamino)-6-(7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)hexahydroindolizin-3(5H)-one
CAS No.:1374240-57-9
Molecular Formula:C₂₀H₂₀ClFN₆O
Molecular Weight:414.87
Hs Code.:

Synonyms:2-(3-chloro-5-fluorophenylamino)-6-(7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)hexahydroindolizin-3(5H)-one

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Chemical Property of 2-(3-chloro-5-fluorophenylamino)-6-(7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)hexahydroindolizin-3(5H)-one

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Technology Process of 2-(3-chloro-5-fluorophenylamino)-6-(7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)hexahydroindolizin-3(5H)-one

There total 5 articles about 2-(3-chloro-5-fluorophenylamino)-6-(7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)hexahydroindolizin-3(5H)-one 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:

: 1374243-50-1
(2S,6R,8aR)-2-(3-chloro-5-fluorophenylamino)-6-(7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)hexahydroindolizin-3(5H)-one

: 1374240-57-9
2-(3-chloro-5-fluorophenylamino)-6-(7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)hexahydroindolizin-3(5H)-one

Guidance literature:: With water; potassium carbonate; In methanol; at 70 ℃; for 24h;

Reference yield:

: 1374243-71-6
methyl 3-(5-aminopyridin-2-yl)-N-(tert-butoxycarbonyl)-L-alaninate

: 1374240-57-9
2-(3-chloro-5-fluorophenylamino)-6-(7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)hexahydroindolizin-3(5H)-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogen; acetic acid / 5% rhodium-on-charcoal / 25 h / 20 °C / 3102.97 Torr

1.2: polymer-supported carbonate rasin / 24 h / 20 °C

2.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 24 h / 90 °C

3.1: hydrogenchloride / 1,4-dioxane; methanol / 23 h / 20 °C

3.2: polymer-supported carbonate resin / 1 h / 20 °C

4.1: copper diacetate / tetrahydrofuran / 0.08 h / Molecular sieve; Inert atmosphere

4.2: 72 h / 20 - 60 °C / Molecular sieve; Inert atmosphere

5.1: potassium carbonate; water / methanol / 24 h / 70 °C

With hydrogenchloride; water; hydrogen; copper diacetate; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; 5% rhodium-on-charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; N,N-dimethyl-formamide;

Reference yield:

: 1374243-46-5
tert-butyl (2S)-6-amino-3-oxooctahydroindolizin-2-ylcarbamate

: 1374240-57-9
2-(3-chloro-5-fluorophenylamino)-6-(7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)hexahydroindolizin-3(5H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 24 h / 90 °C

2.1: hydrogenchloride / 1,4-dioxane; methanol / 23 h / 20 °C

2.2: polymer-supported carbonate resin / 1 h / 20 °C

3.1: copper diacetate / tetrahydrofuran / 0.08 h / Molecular sieve; Inert atmosphere

3.2: 72 h / 20 - 60 °C / Molecular sieve; Inert atmosphere

4.1: potassium carbonate; water / methanol / 24 h / 70 °C

With hydrogenchloride; water; copper diacetate; potassium carbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; 1,4-dioxane; methanol; N,N-dimethyl-formamide;