2-{2-[4-(2,4-Dinitro-phenylsulfanyl)-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl]-ethoxy}-isoindole-1,3-dione

Base Information

Chemical Name:2-{2-[4-(2,4-Dinitro-phenylsulfanyl)-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl]-ethoxy}-isoindole-1,3-dione
CAS No.:190771-73-4
Molecular Formula:C₂₃H₁₆N₆O₇S
Molecular Weight:520.482
Hs Code.:

Synonyms:2-{2-[4-(2,4-Dinitro-phenylsulfanyl)-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl]-ethoxy}-isoindole-1,3-dione

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Chemical Property of 2-{2-[4-(2,4-Dinitro-phenylsulfanyl)-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl]-ethoxy}-isoindole-1,3-dione

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Technology Process of 2-{2-[4-(2,4-Dinitro-phenylsulfanyl)-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl]-ethoxy}-isoindole-1,3-dione

There total 10 articles about 2-{2-[4-(2,4-Dinitro-phenylsulfanyl)-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl]-ethoxy}-isoindole-1,3-dione 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: 81.0%

: 524-38-9
N-hydroxyphthalimide

: 190771-72-3
2-[4-(2,4-Dinitro-phenylsulfanyl)-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl]-ethanol

: 190771-73-4
2-{2-[4-(2,4-Dinitro-phenylsulfanyl)-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl]-ethoxy}-isoindole-1,3-dione

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; for 2h; Ambient temperature;
DOI:10.1039/a606472h

Reference yield:

: 213844-23-6
6-Amino-5-(2-methoxy-tetrahydro-furan-3-yl)-2-thioxo-2,3-dihydro-1H-pyrimidin-4-one

: 190771-73-4
2-{2-[4-(2,4-Dinitro-phenylsulfanyl)-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl]-ethoxy}-isoindole-1,3-dione

Guidance literature:: Multi-step reaction with 8 steps

1: 91 percent / 0.2 M aq. HCl / 4 h / Ambient temperature

2: 92 percent / 35percent aq. ammonia / Raney Ni / 3 h / Heating

3: 65 percent / pyridine / 2 h

4: 36 percent / BzEt₃NCl, POCl₃, PhNMe₂ / acetonitrile / 1 h / Heating

5: 87 percent / NaH / acetonitrile / 1.) 30 min, 2.) 30 min

6: 84 percent / thiourea / ethanol / 1 h / Heating

7: 42 percent / Et₃N / acetonitrile / 0.67 h / Ambient temperature

8: 81 percent / Ph₃P, DEAD / tetrahydrofuran / 2 h / Ambient temperature

With pyridine; hydrogenchloride; ammonium hydroxide; Et₃NBn⁽¹⁺⁾Cl^(1-); sodium hydride; N,N-dimethyl-aniline; triethylamine; thiourea; triphenylphosphine; diethylazodicarboxylate; trichlorophosphate; nickel; In tetrahydrofuran; ethanol; acetonitrile;
DOI:10.1039/a606472h

Reference yield:

: 190771-46-1
5-(2-Hydroxy-ethyl)-2-thioxo-1,2,3,7-tetrahydro-pyrrolo[2,3-d]pyrimidin-4-one

: 190771-73-4
2-{2-[4-(2,4-Dinitro-phenylsulfanyl)-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl]-ethoxy}-isoindole-1,3-dione

Guidance literature:: Multi-step reaction with 7 steps

1: 92 percent / 35percent aq. ammonia / Raney Ni / 3 h / Heating

2: 65 percent / pyridine / 2 h

3: 36 percent / BzEt₃NCl, POCl₃, PhNMe₂ / acetonitrile / 1 h / Heating

4: 87 percent / NaH / acetonitrile / 1.) 30 min, 2.) 30 min

5: 84 percent / thiourea / ethanol / 1 h / Heating

6: 42 percent / Et₃N / acetonitrile / 0.67 h / Ambient temperature

7: 81 percent / Ph₃P, DEAD / tetrahydrofuran / 2 h / Ambient temperature

With pyridine; ammonium hydroxide; Et₃NBn⁽¹⁺⁾Cl^(1-); sodium hydride; N,N-dimethyl-aniline; triethylamine; thiourea; triphenylphosphine; diethylazodicarboxylate; trichlorophosphate; nickel; In tetrahydrofuran; ethanol; acetonitrile;
DOI:10.1039/a606472h