[(3R,4S)-4-(2,5-difluoro-phenyl)-1-(5-{(S)-1-[1-(1H-tetrazol-5-yl)piperidin-4-yl]ethoxy}pyrimidin-2-yl)pyrrolidin-3-yl]carbamic acid tert-butyl ester

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Chemical Name:[(3R,4S)-4-(2,5-difluoro-phenyl)-1-(5-{(S)-1-[1-(1H-tetrazol-5-yl)piperidin-4-yl]ethoxy}pyrimidin-2-yl)pyrrolidin-3-yl]carbamic acid tert-butyl ester
CAS No.:1351343-67-3
Molecular Formula:C₂₇H₃₅F₂N₉O₃
Molecular Weight:571.63
Hs Code.:

Synonyms:[(3R,4S)-4-(2,5-difluoro-phenyl)-1-(5-{(S)-1-[1-(1H-tetrazol-5-yl)piperidin-4-yl]ethoxy}pyrimidin-2-yl)pyrrolidin-3-yl]carbamic acid tert-butyl ester

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Chemical Property of [(3R,4S)-4-(2,5-difluoro-phenyl)-1-(5-{(S)-1-[1-(1H-tetrazol-5-yl)piperidin-4-yl]ethoxy}pyrimidin-2-yl)pyrrolidin-3-yl]carbamic acid tert-butyl ester

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Technology Process of [(3R,4S)-4-(2,5-difluoro-phenyl)-1-(5-{(S)-1-[1-(1H-tetrazol-5-yl)piperidin-4-yl]ethoxy}pyrimidin-2-yl)pyrrolidin-3-yl]carbamic acid tert-butyl ester

There total 5 articles about [(3R,4S)-4-(2,5-difluoro-phenyl)-1-(5-{(S)-1-[1-(1H-tetrazol-5-yl)piperidin-4-yl]ethoxy}pyrimidin-2-yl)pyrrolidin-3-yl]carbamic acid tert-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:

: 1351343-50-4
[(3R,4S)-1-{5-[(S)-1-(1-cyano-piperidin-4-yl)ethoxy]pyrimidin-2-yl}-4-(2,5-difluoro-phenyl)pyrrolidin-3-yl]carbamic acid tert-butyl ester

: 1351343-67-3
[(3R,4S)-4-(2,5-difluoro-phenyl)-1-(5-{(S)-1-[1-(1H-tetrazol-5-yl)piperidin-4-yl]ethoxy}pyrimidin-2-yl)pyrrolidin-3-yl]carbamic acid tert-butyl ester

Guidance literature:: With sodium azide; ammonium chloride; In N,N-dimethyl-formamide; at 20 - 100 ℃; for 16.33h;

Reference yield:

: 832714-37-1
1-[3-(propan-2-yl)-1,2,4-oxadiazol-5-yl]piperidin-4-ol

: 1351343-67-3
[(3R,4S)-4-(2,5-difluoro-phenyl)-1-(5-{(S)-1-[1-(1H-tetrazol-5-yl)piperidin-4-yl]ethoxy}pyrimidin-2-yl)pyrrolidin-3-yl]carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dimethyl sulfoxide / 40 h / 90 °C

2: hydrogen / palladium 10% on activated carbon / ethanol / 1.5 h

3: sodium hydrogencarbonate / dichloromethane; water / 0.75 h / 0 °C

4: sodium azide; ammonium chloride / N,N-dimethyl-formamide / 16.33 h / 20 - 100 °C

With sodium azide; hydrogen; sodium hydrogencarbonate; ammonium chloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; palladium 10% on activated carbon; In ethanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 51075-37-7
4-hydroxypiperidine-1-carbonitrile

: 1351343-67-3
[(3R,4S)-4-(2,5-difluoro-phenyl)-1-(5-{(S)-1-[1-(1H-tetrazol-5-yl)piperidin-4-yl]ethoxy}pyrimidin-2-yl)pyrrolidin-3-yl]carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: zinc(II) chloride / ethanol / 2 h / 20 °C

1.2: 16 h / 50 °C

2.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dimethyl sulfoxide / 40 h / 90 °C

3.1: hydrogen / palladium 10% on activated carbon / ethanol / 1.5 h

4.1: sodium hydrogencarbonate / dichloromethane; water / 0.75 h / 0 °C

5.1: sodium azide; ammonium chloride / N,N-dimethyl-formamide / 16.33 h / 20 - 100 °C

With sodium azide; hydrogen; sodium hydrogencarbonate; ammonium chloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; zinc(II) chloride; palladium 10% on activated carbon; In ethanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide;