2-(2-(aminomethyl)piperidin-1-yl)-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-5-one

Base Information

Chemical Name:2-(2-(aminomethyl)piperidin-1-yl)-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-5-one
CAS No.:1312691-45-4
Molecular Formula:C₁₉H₂₄N₆O
Molecular Weight:352.439
Hs Code.:

Synonyms:2-(2-(aminomethyl)piperidin-1-yl)-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-5-one

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Chemical Property of 2-(2-(aminomethyl)piperidin-1-yl)-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-5-one

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Technology Process of 2-(2-(aminomethyl)piperidin-1-yl)-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-5-one

There total 6 articles about 2-(2-(aminomethyl)piperidin-1-yl)-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-5-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: 17.0%

: 1312691-48-7
tert-butyl (1-(5-oxo-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-yl)piperidin-2-yl)methylcarbamate

: 1312691-45-4
2-(2-(aminomethyl)piperidin-1-yl)-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-5-one

Guidance literature:: tert-butyl (1-(5-oxo-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-yl)piperidin-2-yl)methylcarbamate; With hydrogenchloride; acetic acid; In water; at 20 ℃; for 1h;

With sodium hydrogencarbonate; In water;

Reference yield:

: 1312690-70-2
methyl 2,4-dichloro-6-(m-tolylamino)pyrimidine-5-carboxylate

: 1312691-45-4
2-(2-(aminomethyl)piperidin-1-yl)-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-5-one

Guidance literature:: Multi-step reaction with 4 steps

1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 3 h / 0 °C

2: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide / 1 h / 120 °C / Microwave irradiation

3: hydrogenchloride; hydrogen / palladium on carbon / ethanol; water / 16 h / 20 °C / 760.05 Torr

4: hydrogenchloride; acetic acid / water / 1 h / 20 °C

With hydrogenchloride; hydrogen; acetic acid; N-ethyl-N,N-diisopropylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium on carbon; In ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: 1312690-71-3
2,4-dichloro-6-(m-tolylamino)pyrimidine-5-carboxylic acid

: 1312691-45-4
2-(2-(aminomethyl)piperidin-1-yl)-4-(m-tolylamino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-5-one

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydrogencarbonate / N,N-dimethyl-formamide / 14 h / 0 - 20 °C

2: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 3 h / 0 °C

3: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide / 1 h / 120 °C / Microwave irradiation

4: hydrogenchloride; hydrogen / palladium on carbon / ethanol; water / 16 h / 20 °C / 760.05 Torr

5: hydrogenchloride; acetic acid / water / 1 h / 20 °C

With hydrogenchloride; hydrogen; sodium hydrogencarbonate; acetic acid; N-ethyl-N,N-diisopropylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium on carbon; In ethanol; water; N,N-dimethyl-formamide;