N-[(1R,3r,5S)-9-azabicyclo[3.3.1]non-3-yl]-1-Methyl-1H-indazole-3-carboxaMide hydrochloride

Base Information

• Chemical Name: N-[(1R,3r,5S)-9-azabicyclo[3.3.1]non-3-yl]-1-Methyl-1H-indazole-3-carboxaMide hydrochloride
• CAS No.: 141136-01-8
• Molecular Formula: C₁₇H₂₂N₄O*ClH
• Molecular Weight: 334.849
• Hs Code.: 2933399090
• Mol file: 141136-01-8.mol

Synonyms:Granisetron Related CoMpound C;N-[(1R,3r,5S)-9-azabicyclo[3.3.1]non-3-yl]-1-Methyl-1H-indazole-3-carboxaMide hydrochloride;Granisetron Related Compound C (15 mg) (N-[(1R,3r,5S)-9-azabicyclo[3.3.1]non-3-yl]-1-methyl-1H-indazole-3-carboxamide hydrochloride);9-DesMethyl endo-Granisetron Hydrochloride;1-Methyl-N-[(3-endo)-9-azabicyclo[3.3.1]non-3-yl]-1H-indazole-3-carboxamide hydrochloride;N-Demethyl-endo-granisetron hydrochloride

Chemical Property of N-[(1R,3r,5S)-9-azabicyclo[3.3.1]non-3-yl]-1-Methyl-1H-indazole-3-carboxaMide hydrochloride

Chemical Property:

• Storage Temp.: Hygroscopic, -20°C Freezer, Under inert atmosphere
• Solubility.: DMSO (Slightly), Methanol (Slightly)

Purity/Quality:

99%, ^*data from raw suppliers

9-Desmethylendo-GranisetronHydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Uses: 9-Desmethyl endo-Granisetron hydrochloride (Granisetron USP Related Compound C) is an impurity in the synthesis of Granisetron HCl (G780000), a specific serotonin (5HT3) receptor antagonist. Used as an antiemetic.

Technology Process of N-[(1R,3r,5S)-9-azabicyclo[3.3.1]non-3-yl]-1-Methyl-1H-indazole-3-carboxaMide hydrochloride

There total 1 articles about N-[(1R,3r,5S)-9-azabicyclo[3.3.1]non-3-yl]-1-Methyl-1H-indazole-3-carboxaMide hydrochloride 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: 34.8%

granisetron (109889-09-0,124998-65-8,121061-98-1,1364914-39-5) → endo-N-(9-azabicyclo[3.3.1]non-3-yl)-1-methyl-1H-indazole-3-carboxamide hydrochloride (160177-67-3,141136-01-8)

Guidance literature:

granisetron; With Vinyl chloroformate; In dichloromethane; at 25 - 35 ℃; for 24h;

With hydrogenchloride; In isopropyl alcohol; at 25 ℃; for 1h; Reflux;

DOI:10.2174/157017811799304142

upstream raw materials:

granisetron

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