{4-[4-(4-bromo-phenylcarbamoyl)-2-(7-isopropyl-pyrido[2,3-d]pyrimidin-4-ylamino)-phenylsulfanyl]-phenyl}-carbamic acid 2,2,2-trichloro-ethyl ester

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Chemical Name:{4-[4-(4-bromo-phenylcarbamoyl)-2-(7-isopropyl-pyrido[2,3-d]pyrimidin-4-ylamino)-phenylsulfanyl]-phenyl}-carbamic acid 2,2,2-trichloro-ethyl ester
CAS No.:943772-98-3
Molecular Formula:C₃₂H₂₆BrCl₃N₆O₃S
Molecular Weight:760.926
Hs Code.:

{4-[4-(4-bromo-phenylcarbamoyl)-2-(7-isopropyl-pyrido[2,3-d]pyrimidin-4-ylamino)-phenylsulfanyl]-phenyl}-carbamic acid 2,2,2-trichloro-ethyl ester

Synonyms:{4-[4-(4-bromo-phenylcarbamoyl)-2-(7-isopropyl-pyrido[2,3-d]pyrimidin-4-ylamino)-phenylsulfanyl]-phenyl}-carbamic acid 2,2,2-trichloro-ethyl ester

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Chemical Property of {4-[4-(4-bromo-phenylcarbamoyl)-2-(7-isopropyl-pyrido[2,3-d]pyrimidin-4-ylamino)-phenylsulfanyl]-phenyl}-carbamic acid 2,2,2-trichloro-ethyl ester

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Technology Process of {4-[4-(4-bromo-phenylcarbamoyl)-2-(7-isopropyl-pyrido[2,3-d]pyrimidin-4-ylamino)-phenylsulfanyl]-phenyl}-carbamic acid 2,2,2-trichloro-ethyl ester

There total 10 articles about {4-[4-(4-bromo-phenylcarbamoyl)-2-(7-isopropyl-pyrido[2,3-d]pyrimidin-4-ylamino)-phenylsulfanyl]-phenyl}-carbamic acid 2,2,2-trichloro-ethyl ester 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:

: 943771-00-4
2-bromo-6-isopropyl-nicotinonitrile

: 943772-98-3
{4-[4-(4-bromo-phenylcarbamoyl)-2-(7-isopropyl-pyrido[2,3-d]pyrimidin-4-ylamino)-phenylsulfanyl]-phenyl}-carbamic acid 2,2,2-trichloro-ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: ammonia / ethanol / 20 h / 130 °C

2: toluene / 3 h / Heating / reflux

3: acetic acid / 0.67 h / 140 °C

With ammonia; In ethanol; acetic acid; toluene;

Reference yield:

: 55793-14-1
4-methyl-3-oxo-pentanal; sodium enolate

: 943772-98-3
{4-[4-(4-bromo-phenylcarbamoyl)-2-(7-isopropyl-pyrido[2,3-d]pyrimidin-4-ylamino)-phenylsulfanyl]-phenyl}-carbamic acid 2,2,2-trichloro-ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: water / 0.17 h / 20 °C

1.2: 2 h / Heating / reflux

1.3: pH 4

2.1: tetrabutylammomium bromide; phosphorus pentoxide / toluene / 5 h / Heating / reflux

3.1: ammonia / ethanol / 20 h / 130 °C

4.1: toluene / 3 h / Heating / reflux

5.1: acetic acid / 0.67 h / 140 °C

With tetrabutylammomium bromide; ammonia; phosphorus pentoxide; In ethanol; water; acetic acid; toluene;

Reference yield:

: 106-40-1
4-bromo-aniline

: 943772-98-3
{4-[4-(4-bromo-phenylcarbamoyl)-2-(7-isopropyl-pyrido[2,3-d]pyrimidin-4-ylamino)-phenylsulfanyl]-phenyl}-carbamic acid 2,2,2-trichloro-ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 17 h / 20 °C

2.1: caesium carbonate / N,N-dimethyl-formamide / 4 h / 90 °C

2.2: pH 5

3.1: pyridine / dichloromethane / 16 h

4.1: iron; ammonium chloride / tetrahydrofuran; ethanol; water / 6 h / Heating / reflux

5.1: acetic acid / 0.67 h / 140 °C

With pyridine; iron; ammonium chloride; caesium carbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; dichloromethane; water; acetic acid; N,N-dimethyl-formamide;