5-(4-aminophenyl)-6-morpholin-4-ylmethylthieno[2,3-d]pyrimidin-4-ylamine

Base Information

Chemical Name:5-(4-aminophenyl)-6-morpholin-4-ylmethylthieno[2,3-d]pyrimidin-4-ylamine
CAS No.:866584-80-7
Molecular Formula:C₁₇H₁₉N₅OS
Molecular Weight:341.437
Hs Code.:

Synonyms:5-(4-aminophenyl)-6-morpholin-4-ylmethylthieno[2,3-d]pyrimidin-4-ylamine

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Chemical Property of 5-(4-aminophenyl)-6-morpholin-4-ylmethylthieno[2,3-d]pyrimidin-4-ylamine

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Technology Process of 5-(4-aminophenyl)-6-morpholin-4-ylmethylthieno[2,3-d]pyrimidin-4-ylamine

There total 9 articles about 5-(4-aminophenyl)-6-morpholin-4-ylmethylthieno[2,3-d]pyrimidin-4-ylamine 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:

: 866584-50-1
6-morpholin-4-ylmethyl-5-(4-nitro-phenyl)-thieno[2,3-d]pyrimidin-4-ylamine

: 866584-80-7
5-(4-aminophenyl)-6-morpholin-4-ylmethylthieno[2,3-d]pyrimidin-4-ylamine

Guidance literature:: With iron; ammonium chloride; In tetrahydrofuran; ethanol; at 80 ℃; for 2h;
DOI:10.1021/jm050458h

Reference yield:

: 605661-10-7
2-[1-(4-nitrophenyl)propylidene]malononitrile

: 866584-80-7
5-(4-aminophenyl)-6-morpholin-4-ylmethylthieno[2,3-d]pyrimidin-4-ylamine

Guidance literature:: Multi-step reaction with 7 steps

1.1: 85 percent / Et₂NH; sulfur / ethanol / 1.5 h / 70 °C

2.1: 93 percent / 17 h / 155 °C

3.1: NaH / tetrahydrofuran / 0.17 h / 0 °C

3.2: 63 percent / tetrahydrofuran / 2 h / 0 °C

4.1: N-bromosuccinimide; AIBN / benzene / 3 h / 80 °C

5.1: 476 mg / dimethylformamide / 20 °C

6.1: 98 percent / TFA / CH₂Cl₂ / 1.5 h / 0 °C

7.1: Fe; aq. NH₄Cl / ethanol; tetrahydrofuran / 2 h / 80 °C

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); iron; sodium hydride; ammonium chloride; sulfur; diethylamine; trifluoroacetic acid; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; benzene; 1.1: Gewald reaction;
DOI:10.1021/jm050458h

Reference yield:

: 605661-11-8
2-amino-5-methyl-4-(4-nitrophenyl)thiophene-3-carbonitrile

: 866584-80-7
5-(4-aminophenyl)-6-morpholin-4-ylmethylthieno[2,3-d]pyrimidin-4-ylamine

Guidance literature:: Multi-step reaction with 6 steps

1.1: 93 percent / 17 h / 155 °C

2.1: NaH / tetrahydrofuran / 0.17 h / 0 °C

2.2: 63 percent / tetrahydrofuran / 2 h / 0 °C

3.1: N-bromosuccinimide; AIBN / benzene / 3 h / 80 °C

4.1: 476 mg / dimethylformamide / 20 °C

5.1: 98 percent / TFA / CH₂Cl₂ / 1.5 h / 0 °C

6.1: Fe; aq. NH₄Cl / ethanol; tetrahydrofuran / 2 h / 80 °C

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); iron; sodium hydride; ammonium chloride; trifluoroacetic acid; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm050458h