(5-benzyl-hexahydro-pyrrolo[3,4-c]pyrrol-2-yl)-(4,6-dimethyl-pyrimidin-5-yl)-methanone

Base Information

Chemical Name:(5-benzyl-hexahydro-pyrrolo[3,4-c]pyrrol-2-yl)-(4,6-dimethyl-pyrimidin-5-yl)-methanone
CAS No.:1014702-81-8
Molecular Formula:C₂₀H₂₄N₄O
Molecular Weight:336.437
Hs Code.:

Synonyms:(5-benzyl-hexahydro-pyrrolo[3,4-c]pyrrol-2-yl)-(4,6-dimethyl-pyrimidin-5-yl)-methanone

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Chemical Property of (5-benzyl-hexahydro-pyrrolo[3,4-c]pyrrol-2-yl)-(4,6-dimethyl-pyrimidin-5-yl)-methanone

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Technology Process of (5-benzyl-hexahydro-pyrrolo[3,4-c]pyrrol-2-yl)-(4,6-dimethyl-pyrimidin-5-yl)-methanone

There total 1 articles about (5-benzyl-hexahydro-pyrrolo[3,4-c]pyrrol-2-yl)-(4,6-dimethyl-pyrimidin-5-yl)-methanone 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:

: 86732-22-1
2-benzyloctahydropyrrolo[3,4-c]pyrrole

: 157335-93-8
4,6-dimethylpyrimidine-5-carboxylic acid

: 1014702-81-8
(5-benzyl-hexahydro-pyrrolo[3,4-c]pyrrol-2-yl)-(4,6-dimethyl-pyrimidin-5-yl)-methanone

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃;

Reference yield:

: 1014702-81-8
(5-benzyl-hexahydro-pyrrolo[3,4-c]pyrrol-2-yl)-(4,6-dimethyl-pyrimidin-5-yl)-methanone

: 135865-78-0
(4,6-dimethyl-pyrimidin-5-yl)-(hexahydro-pyrrolo[3,4-c]pyrrol-2-yl)-methanone

Guidance literature:: With ammonium formate; palladium on activated charcoal; In methanol; for 8h; Heating / reflux;

Reference yield:

: 1014702-81-8
(5-benzyl-hexahydro-pyrrolo[3,4-c]pyrrol-2-yl)-(4,6-dimethyl-pyrimidin-5-yl)-methanone

: 1-acetyl-piperidine-4-carboxylic acid (3-chloro-4-methyl-phenyl)-{3-[5-(4,6-dimethyl-pyrimidine-5-carbonyl)-hexahydro-pyrrolo[3,4-c]pyrrol-2-yl]-2,2-dimethyl-propyl}-amide

Guidance literature:: Multi-step reaction with 4 steps

1: ammonium formate / palladium on activated charcoal / methanol / 8 h / Heating / reflux

2: sodium tris(acetoxy)borohydride; acetic acid / dichloromethane / 2 h / 20 °C

3: triethylamine / acetonitrile / 50 °C

4: triethylamine / dichloromethane

With ammonium formate; sodium tris(acetoxy)borohydride; acetic acid; triethylamine; palladium on activated charcoal; In methanol; dichloromethane; acetonitrile;