tert-butyl (1S,2R)-2-(5-oxo-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-ylamino)cyclohexylcarbamate

Base Information

Chemical Name:tert-butyl (1S,2R)-2-(5-oxo-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-ylamino)cyclohexylcarbamate
CAS No.:1312690-69-9
Molecular Formula:C₂₄H₃₂N₆O₃
Molecular Weight:452.556
Hs Code.:

Synonyms:tert-butyl (1S,2R)-2-(5-oxo-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-ylamino)cyclohexylcarbamate

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Chemical Property of tert-butyl (1S,2R)-2-(5-oxo-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-ylamino)cyclohexylcarbamate

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Technology Process of tert-butyl (1S,2R)-2-(5-oxo-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-ylamino)cyclohexylcarbamate

There total 5 articles about tert-butyl (1S,2R)-2-(5-oxo-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-ylamino)cyclohexylcarbamate 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: 83.0%

: 1312690-68-8
ethyl 2-((1R,2S)-2-(tert-butoxycarbonylamino)cyclohexylamino)-4-((1,3-dioxoisoindolin-2-yl)methyl)-6-(m-tolylamino)pyrimidine-5-carboxylate

: 1312690-69-9
tert-butyl (1S,2R)-2-(5-oxo-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-ylamino)cyclohexylcarbamate

Guidance literature:: With ethanol; hydrazine hydrate; at 65 ℃; for 12h;

Reference yield:

: 1312690-64-4
ethyl 2,4-dichloro-6-((1,3-dioxoisoindolin-2-yl)methyl)pyrimidine-5-carboxylate

: 1312690-69-9
tert-butyl (1S,2R)-2-(5-oxo-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-ylamino)cyclohexylcarbamate

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / acetonitrile / 12 h / 20 °C

2: triethylamine / ISOPROPYLAMIDE / 3 h / 80 °C

3: ethanol; hydrazine hydrate / 12 h / 65 °C

With ethanol; hydrazine hydrate; triethylamine; N-ethyl-N,N-diisopropylamine; In ISOPROPYLAMIDE; acetonitrile;

Reference yield:

: 1312690-66-6
ethyl 6-((1,3-dioxoisoindolin-2-yl)methyl)-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

: 1312690-69-9
tert-butyl (1S,2R)-2-(5-oxo-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-ylamino)cyclohexylcarbamate

Guidance literature:: Multi-step reaction with 4 steps

1: trichlorophosphate / 12 h / 100 °C

2: N-ethyl-N,N-diisopropylamine / acetonitrile / 12 h / 20 °C

3: triethylamine / ISOPROPYLAMIDE / 3 h / 80 °C

4: ethanol; hydrazine hydrate / 12 h / 65 °C

With ethanol; hydrazine hydrate; triethylamine; N-ethyl-N,N-diisopropylamine; trichlorophosphate; In ISOPROPYLAMIDE; acetonitrile;