rac-2-(1-amino-ethyl)-3-(4-ethoxy-phenyl)-3H-pyrido[2,3-d]pyrimidin-4-one

Base Information

Chemical Name:rac-2-(1-amino-ethyl)-3-(4-ethoxy-phenyl)-3H-pyrido[2,3-d]pyrimidin-4-one
CAS No.:947536-13-2
Molecular Formula:C₁₇H₁₈N₄O₂
Molecular Weight:310.356
Hs Code.:

Synonyms:rac-2-(1-amino-ethyl)-3-(4-ethoxy-phenyl)-3H-pyrido[2,3-d]pyrimidin-4-one

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Chemical Property of rac-2-(1-amino-ethyl)-3-(4-ethoxy-phenyl)-3H-pyrido[2,3-d]pyrimidin-4-one

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Technology Process of rac-2-(1-amino-ethyl)-3-(4-ethoxy-phenyl)-3H-pyrido[2,3-d]pyrimidin-4-one

There total 5 articles about rac-2-(1-amino-ethyl)-3-(4-ethoxy-phenyl)-3H-pyrido[2,3-d]pyrimidin-4-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:

: 5345-47-1
2-aminopyridin-3-carboxylic acid

: 947536-13-2
rac-2-(1-amino-ethyl)-3-(4-ethoxy-phenyl)-3H-pyrido[2,3-d]pyrimidin-4-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-methylmorpholine; iso-butyl chloroformate / CH₂Cl₂

1.2: CH₂Cl₂ / -20 - 20 °C

2.1: CH₂Cl₂ / -20 - 20 °C

3.1: 64 percent / N-methylmorpholine; isobutyl chloroformate / CH₂Cl₂ / -20 - 20 °C

4.1: 100 percent / trifluoroacetic acid / CH₂Cl₂ / 4 h / 20 °C

With 4-methyl-morpholine; trifluoroacetic acid; isobutyl chloroformate; In dichloromethane;
DOI:10.1002/ardp.200700037

Reference yield:

: 473720-90-0
(R)-{1-[3-(4-ethoxy-phenylcarbamoyl)-pyridin-2-ylcarbamoyl]-ethyl}-carbamic acid tert-butyl ester

: 947536-13-2
rac-2-(1-amino-ethyl)-3-(4-ethoxy-phenyl)-3H-pyrido[2,3-d]pyrimidin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: 64 percent / N-methylmorpholine; isobutyl chloroformate / CH₂Cl₂ / -20 - 20 °C

2: 100 percent / trifluoroacetic acid / CH₂Cl₂ / 4 h / 20 °C

With 4-methyl-morpholine; trifluoroacetic acid; isobutyl chloroformate; In dichloromethane;
DOI:10.1002/ardp.200700037

Reference yield:

: 473720-89-7
(R)-[1-(4-oxo-4H-pyrido[2,3-d][1,3]oxazin-2-yl)-ethyl]-carbamic acid tert-butyl ester

: 947536-13-2
rac-2-(1-amino-ethyl)-3-(4-ethoxy-phenyl)-3H-pyrido[2,3-d]pyrimidin-4-one

Guidance literature:: Multi-step reaction with 3 steps

1: CH₂Cl₂ / -20 - 20 °C

2: 64 percent / N-methylmorpholine; isobutyl chloroformate / CH₂Cl₂ / -20 - 20 °C

3: 100 percent / trifluoroacetic acid / CH₂Cl₂ / 4 h / 20 °C

With 4-methyl-morpholine; trifluoroacetic acid; isobutyl chloroformate; In dichloromethane;
DOI:10.1002/ardp.200700037