N-[1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-4-piperidinyl]-3-{[2-(1-pyrrolidinyl)ethyl]oxy}benzamide

Base Information

Chemical Name:N-[1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-4-piperidinyl]-3-{[2-(1-pyrrolidinyl)ethyl]oxy}benzamide
CAS No.:1383342-13-9
Molecular Formula:C₂₅H₃₂N₆O₂
Molecular Weight:448.568
Hs Code.:

Synonyms:N-[1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-4-piperidinyl]-3-{[2-(1-pyrrolidinyl)ethyl]oxy}benzamide

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Chemical Property of N-[1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-4-piperidinyl]-3-{[2-(1-pyrrolidinyl)ethyl]oxy}benzamide

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Technology Process of N-[1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-4-piperidinyl]-3-{[2-(1-pyrrolidinyl)ethyl]oxy}benzamide

There total 5 articles about N-[1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-4-piperidinyl]-3-{[2-(1-pyrrolidinyl)ethyl]oxy}benzamide 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:

: 1383342-60-6
1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-4-piperidinamine hydrochloride

: 3-{[2-(1-pyrrolidinyl)ethyl]oxy}benzoic acid

: 1383342-13-9
N-[1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-4-piperidinyl]-3-{[2-(1-pyrrolidinyl)ethyl]oxy}benzamide

Guidance literature:: 3-{[2-(1-pyrrolidinyl)ethyl]oxy}benzoic acid; With 4-methyl-morpholine; 2-chloro-4,6-dimethoxy-1 ,3,5-triazine; In acetonitrile; at 0 ℃; for 2h; Inert atmosphere;

1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-4-piperidinamine hydrochloride; In acetonitrile; at 0 - 20 ℃; for 16h;

Reference yield:

: 262425-12-7
methyl 3-[2-(1-pyrrolidinyl)ethoxy]benzoate

: 1383342-13-9
N-[1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-4-piperidinyl]-3-{[2-(1-pyrrolidinyl)ethyl]oxy}benzamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydroxide; water / methanol / 18 h / Reflux

1.2: pH 3

2.1: 4-methyl-morpholine; 2-chloro-4,6-dimethoxy-1 ,3,5-triazine / acetonitrile / 2 h / 0 °C / Inert atmosphere

2.2: 16 h / 0 - 20 °C

With 4-methyl-morpholine; 2-chloro-4,6-dimethoxy-1 ,3,5-triazine; water; sodium hydroxide; In methanol; acetonitrile;

Reference yield:

: 5050-41-9
N-(2-chloroethyl)-pyrrolidine

: 1383342-13-9
N-[1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-4-piperidinyl]-3-{[2-(1-pyrrolidinyl)ethyl]oxy}benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate; potassium iodide / acetone / 48 h / Reflux

2.1: sodium hydroxide; water / methanol / 18 h / Reflux

2.2: pH 3

3.1: 4-methyl-morpholine; 2-chloro-4,6-dimethoxy-1 ,3,5-triazine / acetonitrile / 2 h / 0 °C / Inert atmosphere

3.2: 16 h / 0 - 20 °C

With 4-methyl-morpholine; 2-chloro-4,6-dimethoxy-1 ,3,5-triazine; water; potassium carbonate; potassium iodide; sodium hydroxide; In methanol; acetone; acetonitrile;