methanesulfonic acid 3-{4-[tert-butoxycarbonyl-(4-cyano-2-methyl-phenyl)-amino]-6-chloro-2-methyl-pyrimidin-5-yl}-4-(tert-butyl-diphenyl-silanyloxy)-butyl ester

Base Information

Chemical Name:methanesulfonic acid 3-{4-[tert-butoxycarbonyl-(4-cyano-2-methyl-phenyl)-amino]-6-chloro-2-methyl-pyrimidin-5-yl}-4-(tert-butyl-diphenyl-silanyloxy)-butyl ester
CAS No.:862901-72-2
Molecular Formula:C₃₉H₄₇ClN₄O₆SSi
Molecular Weight:763.43
Hs Code.:

methanesulfonic acid 3-{4-[<i>tert</i>-butoxycarbonyl-(4-cyano-2-methyl-phenyl)-amino]-6-chloro-2-methyl-pyrimidin-5-yl}-4-(<i>tert</i>-butyl-diphenyl-silanyloxy)-butyl ester

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Chemical Property of methanesulfonic acid 3-{4-[tert-butoxycarbonyl-(4-cyano-2-methyl-phenyl)-amino]-6-chloro-2-methyl-pyrimidin-5-yl}-4-(tert-butyl-diphenyl-silanyloxy)-butyl ester

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Technology Process of methanesulfonic acid 3-{4-[tert-butoxycarbonyl-(4-cyano-2-methyl-phenyl)-amino]-6-chloro-2-methyl-pyrimidin-5-yl}-4-(tert-butyl-diphenyl-silanyloxy)-butyl ester

There total 9 articles about methanesulfonic acid 3-{4-[tert-butoxycarbonyl-(4-cyano-2-methyl-phenyl)-amino]-6-chloro-2-methyl-pyrimidin-5-yl}-4-(tert-butyl-diphenyl-silanyloxy)-butyl 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:

: {5-[1-(tert-butyl-diphenyl-silanyloxymethyl)-3-hydroxy-propyl]-6-chloro-2-methyl-pyrimidin-4-yl}-(4-cyano-2-methyl-phenyl)-carbamic acid tert-butyl ester

: 124-63-0
methanesulfonyl chloride

: 862901-72-2
methanesulfonic acid 3-{4-[tert-butoxycarbonyl-(4-cyano-2-methyl-phenyl)-amino]-6-chloro-2-methyl-pyrimidin-5-yl}-4-(tert-butyl-diphenyl-silanyloxy)-butyl ester

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 18h;
DOI:10.1016/j.bmcl.2005.05.040

Reference yield:

: (4,6-dihydroxy-2-methyl-pyrimidin-5-yl)-acetic acid ethyl ester

: 862901-72-2
methanesulfonic acid 3-{4-[tert-butoxycarbonyl-(4-cyano-2-methyl-phenyl)-amino]-6-chloro-2-methyl-pyrimidin-5-yl}-4-(tert-butyl-diphenyl-silanyloxy)-butyl ester

Guidance literature:: Multi-step reaction with 8 steps

1.1: 73 percent / POCl₃ / 3.5 h / Heating

2.1: 68 percent / LiHMDS / hexane; tetrahydrofuran / 0 - 20 °C

3.1: 86 percent / DIBAl-H / hexane; CH₂Cl₂ / 3 h / -78 - 0 °C

4.1: 90 percent / imidazole; DMAP / dimethylformamide / 2 h / 0 - 20 °C

5.1: NaH / tetrahydrofuran / 0.5 h / 0 °C

5.2: tetrahydrofuran / 5 h / Heating

6.1: DMAP / CH₂Cl₂ / 48 h / 20 °C

7.1: O₃ / CH₂Cl₂ / 0.5 h / -78 °C

7.2: NaBH₄ / CH₂Cl₂ / 3 h / 20 °C

8.1: Et₃N / CH₂Cl₂ / 18 h / 20 °C

With 1H-imidazole; dmap; sodium hydride; diisobutylaluminium hydride; ozone; triethylamine; lithium hexamethyldisilazane; trichlorophosphate; In tetrahydrofuran; hexane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2005.05.040

Reference yield:

: 474103-23-6
2-(4,6-dichloro-2-methyl-pyrimidin-5-yl)-pent-4-en-1-ol

: 862901-72-2
methanesulfonic acid 3-{4-[tert-butoxycarbonyl-(4-cyano-2-methyl-phenyl)-amino]-6-chloro-2-methyl-pyrimidin-5-yl}-4-(tert-butyl-diphenyl-silanyloxy)-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 90 percent / imidazole; DMAP / dimethylformamide / 2 h / 0 - 20 °C

2.1: NaH / tetrahydrofuran / 0.5 h / 0 °C

2.2: tetrahydrofuran / 5 h / Heating

3.1: DMAP / CH₂Cl₂ / 48 h / 20 °C

4.1: O₃ / CH₂Cl₂ / 0.5 h / -78 °C

4.2: NaBH₄ / CH₂Cl₂ / 3 h / 20 °C

5.1: Et₃N / CH₂Cl₂ / 18 h / 20 °C

With 1H-imidazole; dmap; sodium hydride; ozone; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2005.05.040