tert-butyl (1-(4-(2-amino-4-methoxy-5-phenylfuro[2,3-d]pyrimidin-6-yl)phenyl)cyclobutyl)carbamate

Base Information

Chemical Name:tert-butyl (1-(4-(2-amino-4-methoxy-5-phenylfuro[2,3-d]pyrimidin-6-yl)phenyl)cyclobutyl)carbamate
CAS No.:1301611-09-5
Molecular Formula:C₂₈H₃₀N₄O₄
Molecular Weight:486.571
Hs Code.:

Synonyms:tert-butyl (1-(4-(2-amino-4-methoxy-5-phenylfuro[2,3-d]pyrimidin-6-yl)phenyl)cyclobutyl)carbamate

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Chemical Property of tert-butyl (1-(4-(2-amino-4-methoxy-5-phenylfuro[2,3-d]pyrimidin-6-yl)phenyl)cyclobutyl)carbamate

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Technology Process of tert-butyl (1-(4-(2-amino-4-methoxy-5-phenylfuro[2,3-d]pyrimidin-6-yl)phenyl)cyclobutyl)carbamate

There total 7 articles about tert-butyl (1-(4-(2-amino-4-methoxy-5-phenylfuro[2,3-d]pyrimidin-6-yl)phenyl)cyclobutyl)carbamate 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: 63.0%

: 1301610-66-1
tert-butyl (1-(4-(4-methoxy-2-(methylsulfonyl)-5-phenylfuro[2,3-d]pyrimidin-6-yl)phenyl)cyclobutyl)carbamate

: 1301611-09-5
tert-butyl (1-(4-(2-amino-4-methoxy-5-phenylfuro[2,3-d]pyrimidin-6-yl)phenyl)cyclobutyl)carbamate

Guidance literature:: With ammonium hydroxide; at 80 ℃; for 48h; Product distribution / selectivity; Sealed tube;

Reference yield:

: 10428-49-6
β-chloro-β-nitrostyrene

: 1301611-09-5
tert-butyl (1-(4-(2-amino-4-methoxy-5-phenylfuro[2,3-d]pyrimidin-6-yl)phenyl)cyclobutyl)carbamate

Guidance literature:: Multi-step reaction with 7 steps

1.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / ethanol / 96 h / Inert atmosphere; Reflux

2.1: trichlorophosphate / 1.5 h / Reflux

3.1: N,N-dimethyl-formamide / 1.5 h / 80 °C / Inert atmosphere

4.1: n-butyllithium / tetrahydrofuran; hexanes / 1 h / -78 °C / Inert atmosphere

4.2: 1 h / -78 °C / Inert atmosphere

4.3: 20 °C / Inert atmosphere

5.1: potassium phosphate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide; water / 1.5 h / 90 °C / Inert atmosphere

6.1: Oxone / water; tetrahydrofuran; methanol / 20 - 50 °C

7.1: ammonium hydroxide / 48 h / 80 °C / Sealed tube

With Oxone; ammonium hydroxide; potassium phosphate; n-butyllithium; 1,8-diazabicyclo[5.4.0]undec-7-ene; trichlorophosphate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; methanol; hexanes; ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: 1301610-61-6
2-methylthio-5-phenylfuro[2,3-d]pyrimidin-4(3H)-one

: 1301611-09-5
tert-butyl (1-(4-(2-amino-4-methoxy-5-phenylfuro[2,3-d]pyrimidin-6-yl)phenyl)cyclobutyl)carbamate

Guidance literature:: Multi-step reaction with 6 steps

1.1: trichlorophosphate / 1.5 h / Reflux

2.1: N,N-dimethyl-formamide / 1.5 h / 80 °C / Inert atmosphere

3.1: n-butyllithium / tetrahydrofuran; hexanes / 1 h / -78 °C / Inert atmosphere

3.2: 1 h / -78 °C / Inert atmosphere

3.3: 20 °C / Inert atmosphere

4.1: potassium phosphate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide; water / 1.5 h / 90 °C / Inert atmosphere

5.1: Oxone / water; tetrahydrofuran; methanol / 20 - 50 °C

6.1: ammonium hydroxide / 48 h / 80 °C / Sealed tube

With Oxone; ammonium hydroxide; potassium phosphate; n-butyllithium; trichlorophosphate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; methanol; hexanes; water; N,N-dimethyl-formamide;