tert-butyl 4-(4-[4-(1H-tetrazol-1-yl)phenoxy]furo[3,2-d]pyrimidin-7-yl)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(4-[4-(1H-tetrazol-1-yl)phenoxy]furo[3,2-d]pyrimidin-7-yl)piperidine-1-carboxylate
CAS No.:1353005-07-8
Molecular Formula:C₂₃H₂₅N₇O₄
Molecular Weight:463.496
Hs Code.:

Synonyms:tert-butyl 4-(4-[4-(1H-tetrazol-1-yl)phenoxy]furo[3,2-d]pyrimidin-7-yl)piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-(4-[4-(1H-tetrazol-1-yl)phenoxy]furo[3,2-d]pyrimidin-7-yl)piperidine-1-carboxylate

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Technology Process of tert-butyl 4-(4-[4-(1H-tetrazol-1-yl)phenoxy]furo[3,2-d]pyrimidin-7-yl)piperidine-1-carboxylate

There total 9 articles about tert-butyl 4-(4-[4-(1H-tetrazol-1-yl)phenoxy]furo[3,2-d]pyrimidin-7-yl)piperidine-1-carboxylate 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: 70.0%

: 64001-11-2
1-(4-hydroxyphenyl)-1H-1,2,3,4-tetrazole

: 1353005-11-4
tert-butyl 4-{4-[(1H-benzo[d][1,2,3]triazol-1-yl)oxy]furo[3,2-d]pyrimidin-7-yl}piperidine-1-carboxylate

: 1353005-07-8
tert-butyl 4-(4-[4-(1H-tetrazol-1-yl)phenoxy]furo[3,2-d]pyrimidin-7-yl)piperidine-1-carboxylate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 70 ℃; for 5h;

Reference yield:

: 123855-51-6
tert-butyl 4-(hydroxymethyl)piperidin-1-carboxylate

: 1353005-07-8
tert-butyl 4-(4-[4-(1H-tetrazol-1-yl)phenoxy]furo[3,2-d]pyrimidin-7-yl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1: triethylamine / tetrahydrofuran; water / 0.67 h / Inert atmosphere; Cooling with ice

2: water; ethanol / 24 h / 80 °C

3: potassium tert-butylate / water; N,N-dimethyl-formamide / 20 °C / Inert atmosphere; Cooling with ice

4: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 20 °C

5: ethanol / 48 h / Reflux

6: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 0.67 h / 20 °C / Inert atmosphere

7: potassium carbonate / N,N-dimethyl-formamide / 5 h / 70 °C

With potassium tert-butylate; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: 161975-39-9
tert-butyl 4-(((methylsulfonyl)oxy)methyl)piperidine-1-carboxylate

: 1353005-07-8
tert-butyl 4-(4-[4-(1H-tetrazol-1-yl)phenoxy]furo[3,2-d]pyrimidin-7-yl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1: water; ethanol / 24 h / 80 °C

2: potassium tert-butylate / water; N,N-dimethyl-formamide / 20 °C / Inert atmosphere; Cooling with ice

3: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 20 °C

4: ethanol / 48 h / Reflux

5: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 0.67 h / 20 °C / Inert atmosphere

6: potassium carbonate / N,N-dimethyl-formamide / 5 h / 70 °C

With potassium tert-butylate; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide;