N-Allyl-1,7-dideazaadenine

Base Information

• Chemical Name: N-Allyl-1,7-dideazaadenine
• CAS No.: 640735-22-4
• Molecular Formula: C10H11N3
• Molecular Weight: 173.217
• Hs Code.: 2933990090
• Mol file: 640735-22-4.mol

Synonyms:

Chemical Property of N-Allyl-1,7-dideazaadenine

Chemical Property:

• PSA: 40.71000
• LogP: 2.23380
• Solubility.: Chloroform, Dichloromethane, 1,4-DIoxane; Ethyl Acetate, Methanol

Purity/Quality:

N-Allyl-1,7-dideazaadenine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Uses: N-Allyl-1,7-dideazaadenine is used in the preparation of pyrrolotriazines.

Technology Process of N-Allyl-1,7-dideazaadenine

There total 1 articles about N-Allyl-1,7-dideazaadenine 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:

1-amino-2-propene (107-11-9,30551-89-4) + 4-chloro-7-azaindole (55052-28-3) → allyl-(1H-pyrrolo[2,3-b]pyridin-4-yl)amine (640735-22-4)

Guidance literature:

With palladium diacetate; sodium t-butanolate; CyJohnPhos; In 1,4-dioxane; at 100 ℃; for 16h;

DOI:10.1021/ol036030z

Reference yield:

allyl-(1H-pyrrolo[2,3-b]pyridin-4-yl)amine (640735-22-4) → 4-fluoro-1H-pyrrolo[2,3-b]pyridine (640735-23-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 13.15 g / methanesulfonic acid / Pd/C / ethanol / 72 h / 105 °C

2: 44 percent / tetrafluoroboric acid; sodium nitrite / H₂O / 22 h / 0 - 20 °C

With tetrafluoroboric acid; methanesulfonic acid; sodium nitrite; palladium on activated charcoal; In ethanol; water; 2: Balz-Schiemann reaction;

DOI:10.1021/ol036030z

upstream raw materials:

1-amino-2-propene

4-chloro-7-azaindole

Downstream raw materials:

4-fluoro-1H-pyrrolo[2,3-b]pyridine

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