[5-phenyl-7-(2,2,6-trimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-p-tolyl-amine

Base Information

• Chemical Name: [5-phenyl-7-(2,2,6-trimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-p-tolyl-amine
• CAS No.: 291759-36-9
• Molecular Formula: C₂₇H₂₈N₄O₃
• Molecular Weight: 456.544

Synonyms:[5-phenyl-7-(2,2,6-trimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-p-tolyl-amine

Chemical Property of [5-phenyl-7-(2,2,6-trimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-p-tolyl-amine

Chemical Property:

Purity/Quality:

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Technology Process of [5-phenyl-7-(2,2,6-trimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-p-tolyl-amine

There total 4 articles about [5-phenyl-7-(2,2,6-trimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-p-tolyl-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: 68.0%

5-deoxy-2,3-O-isopropylidene-α/β-D-ribofuranosyl chloride + 4-N-(4-methylphenyl)amino-5-phenylpyrrolo[2,3-d]pyrimidine (291759-33-6) → [5-phenyl-7-(2,2,6-trimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-p-tolyl-amine (291759-36-9)

Guidance literature:

With potassium hydroxide; In toluene; at 20 ℃;

DOI:10.1021/jm0000259

Reference yield:

2-amino-3-cyano-4-phenylpyrrole (54153-51-4) → [5-phenyl-7-(2,2,6-trimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-p-tolyl-amine (291759-36-9)

Guidance literature:

Multi-step reaction with 4 steps

1: p-toluenesulfonic acid / tetrahydrofuran / 0.5 h / Heating

2: dimethylformamide / 0.75 h / Heating

3: H₂O / 8 h / Heating

4: 68 percent / KOH; TDA-1 / toluene / 20 °C

With potassium hydroxide; toluene-4-sulfonic acid; In tetrahydrofuran; water; N,N-dimethyl-formamide; toluene; 1: ethoxylation / 2: cyclocondensation / 3: Rearrangement / 4: glycosylation;

DOI:10.1021/jm0000259

Reference yield:

2-ethoxymethyleneimino-4-phenylpyrrole-3-carbonitrile (186300-70-9) → [5-phenyl-7-(2,2,6-trimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-p-tolyl-amine (291759-36-9)

Guidance literature:

Multi-step reaction with 3 steps

1: dimethylformamide / 0.75 h / Heating

2: H₂O / 8 h / Heating

3: 68 percent / KOH; TDA-1 / toluene / 20 °C

With potassium hydroxide; In water; N,N-dimethyl-formamide; toluene; 1: cyclocondensation / 2: Rearrangement / 3: glycosylation;

DOI:10.1021/jm0000259

upstream raw materials:

4-N-(4-methylphenyl)amino-5-phenylpyrrolo[2,3-d]pyrimidine

2-amino-3-cyano-4-phenylpyrrole

2-ethoxymethyleneimino-4-phenylpyrrole-3-carbonitrile

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