461052-23-3

Basic information

• Product Name: 1-[2-(1-benzyloxycarbonyl-piperidin-4-yl)-ethyl]-1H-indole-3-carboxylic acid methyl ester
• Synonyms: 1-[2-(1-benzyloxycarbonyl-piperidin-4-yl)-ethyl]-1H-indole-3-carboxylic acid methyl ester
• CAS NO: 461052-23-3
• Molecular Weight: 420.508
• Mol File: 461052-23-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-[2-(1-benzyloxycarbonyl-piperidin-4-yl)-ethyl]-1H-indole-3-carboxylic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[2-(1-benzyloxycarbonyl-piperidin-4-yl)-ethyl]-1H-indole-3-carboxylic acid methyl ester(461052-23-3)
• EPA Substance Registry System: 1-[2-(1-benzyloxycarbonyl-piperidin-4-yl)-ethyl]-1H-indole-3-carboxylic acid methyl ester(461052-23-3)

Safety Data

• Hazardous Substances Data: 461052-23-3(Hazardous Substances Data)

Upstream product

• 115909-91-6 1-(Benzyloxycarbonyl)-4-(2-hydroxyethyl)piperidine 
• 942-24-5 3-methoxycarbonylindole 
• 120426-39-3 2-(N-Benzyloxycarbonylpiperidin-4-yl)ethyl iodide 

Downstream Products

• 461052-32-4 1-[2-(1-benzyloxycarbonyl-piperidin-4-yl)-ethyl]-1H-indole-3-carboxylic acid 
• 461052-38-0 4-{2-[3-(2-ethoxycarbonyl-ethylcarbamoyl)-indol-1-yl]-ethyl}-piperidine-1-carboxylic acid benzyl ester 

Relevant articles and documents

Design and synthesis of a series of indole glycoprotein IIb/IIIa inhibitors

Synthesis of 1,3-disubstituted indoles derivatives as potential glycoprotein (GP) IIb/IIIa antagonists was reported. Substitution of the indolic nitrogen atom by piperidino or benzamidino moieties was used as mimics of an arginine residue. The acid carboxylic group was linked to the indole scaffold in position-3 via a methylene unit (compounds 4, 9, 10). Introduction of a β-alanine chain was carried out on the acids (17-22) which after deprotection and basic hydrolysis afforded the final compounds 39-46. The distance between the indole scaffold and the amide bond was modulated from no methylene unit (compound 39) to 1 (compounds 40, 41) or 2 methylene units (compounds 42-46). The presence of a tosylamino group on the β-alanine chain (compound 56) slightly increased the inhibiting action on platelet aggregation initiated by collagen.