6-bromo-N-(3-(4-methoxybenzyloxy)phenyl)thieno[3,2-d]pyrimidin-4-amine

Base Information

Chemical Name:6-bromo-N-(3-(4-methoxybenzyloxy)phenyl)thieno[3,2-d]pyrimidin-4-amine
CAS No.:1228102-67-7
Molecular Formula:C₂₀H₁₆BrN₃O₂S
Molecular Weight:442.336
Hs Code.:

Synonyms:6-bromo-N-(3-(4-methoxybenzyloxy)phenyl)thieno[3,2-d]pyrimidin-4-amine

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Chemical Property of 6-bromo-N-(3-(4-methoxybenzyloxy)phenyl)thieno[3,2-d]pyrimidin-4-amine

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Technology Process of 6-bromo-N-(3-(4-methoxybenzyloxy)phenyl)thieno[3,2-d]pyrimidin-4-amine

There total 8 articles about 6-bromo-N-(3-(4-methoxybenzyloxy)phenyl)thieno[3,2-d]pyrimidin-4-amine 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: 80.0%

: 131770-85-9
3-[(4-methoxybenzyl)oxy]aniline

: 225385-03-5
6-bromo-4-chlorothiopheno[3,2-D]pyrimidine

: 1228102-67-7
6-bromo-N-(3-(4-methoxybenzyloxy)phenyl)thieno[3,2-d]pyrimidin-4-amine

Guidance literature:: In 1,2-dichloro-ethane; tert-butyl alcohol; at 85 ℃; for 72h; Sealed tube;

Reference yield:

: 1-(4-methoxybenzyloxy)-3-nitrobenzene

: 1228102-67-7
6-bromo-N-(3-(4-methoxybenzyloxy)phenyl)thieno[3,2-d]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 2 steps

1: iron; water / methanol / 15 h / Reflux

2: 1,2-dichloro-ethane; tert-butyl alcohol / 72 h / 85 °C / Sealed tube

With water; iron; In methanol; 1,2-dichloro-ethane; tert-butyl alcohol;

Reference yield:

: 22288-78-4
Methyl 3-aminothiophene-2-carboxylate

: 1228102-67-7
6-bromo-N-(3-(4-methoxybenzyloxy)phenyl)thieno[3,2-d]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 5 steps

1.1: ammonium acetate / 4 h / Reflux

2.1: ammonium formate / formamide / 20 h / 140 °C

3.1: oxalyl dichloride; N,N-dimethyl-formamide / 1,2-dichloro-ethane / 2.5 h / Reflux

4.1: lithium diisopropyl amide / tetrahydrofuran / 0.33 h / -78 °C

4.2: 2.33 h / -78 - 20 °C

5.1: 1,2-dichloro-ethane; tert-butyl alcohol / 72 h / 85 °C / Sealed tube

With oxalyl dichloride; ammonium acetate; ammonium formate; N,N-dimethyl-formamide; lithium diisopropyl amide; In tetrahydrofuran; formamide; 1,2-dichloro-ethane; tert-butyl alcohol;