61085-47-0

Usage

InChI:InChI=1/C19H22N2O2.Na/c22-18(23)19(20-17-9-5-2-6-10-17)11-13-21(14-12-19)15-16-7-3-1-4-8-16;/h1-10,20H,11-15H2,(H,22,23);/q;+1/p-1

Upstream product

• 3612-20-2 1-phenylmethyl-4-piperidone 
• 62-53-3 aniline 
• 968-86-5 1-benzyl-4-(phenylamino)piperidine-4-carbonitrile 
• 127354-23-8 C₂₀H₂₁ClN₄O₃S 
• 127354-24-9 8-Benzyl-1-phenyl-1,3,8-triazaspiro[4.5]decane-2,4-dione 
• 1096-03-3 1-benzyl-4-phenylaminopiperidine-4-carboxylic acid amide 

Downstream Products

• 61085-60-7 methyl 4-(phenylamino)-1-(phenylmethyl)-4-piperidinecarboxylate 
• 61085-63-0 propyl 4-(phenylamino)-1-(phenylmethyl)-4-piperidinecarboxylate ethanedioate 
• 690273-72-4 4-(benzoyl-phenylamino)-1-benzylpiperidine-4-carboxylic acid benzyl ester 
• 690272-32-3 1-benzyl-4-[(3-methylbutanoyl)(phenyl)amino]piperidine-4-carboxylic acid ethyl ester 
• 61085-72-1 methyl 4-[N-(1-oxopropyl)-N-phenylamino]-1-benzyl-4-piperidinecarboxylate 
• 61085-87-8 methyl 4-[N-(1-oxopropyl)-N-phenylamino]-4-piperidinecarboxylate hydrochloride 
• 256507-84-3 1-benzyl-4-[phenyl(propionyl)amino]piperidine-4-carboxylic acid 

Relevant academic research and scientific papers

SUBSTITUTED 4-AMINO-PIPERIDINES

The present invention relates to new substituted 4-amino-piperidine opioid receptor modulators, pharmaceutical compositions thereof, and methods of use thereof

IMPROVED METHOD OF MAKING SUFENTANIL

The present invention relates to a process for the preparation of piperidine derivatives including sufentanil and its pharmaceutically acceptable salts, such as it citrate salt

RECEPTOR REGULATOR

A compound having a partial structure represented by the formula (A) (wherein ring Xa represents a nitrogen-containing ring and R represents optionally substituted amino) or a salt thereof. The compound or salt is highly effective in regulating neuromedin U receptors and is useful as a preventive/therapeutic agent for hypertension, etc.

Preparation of substituted alkali metal piperidine-4-carboxylates

A method of preparing certain substituted alkali metal 4-carboxy-piperidine salts (I) by alkaline hydrolysis of certain novel substituted 1,3,8-triazaspiro[4.5]decane-2, 4-diones (IV) which in turn are obtained from certain novel substituted chlorosulphon

N-(4-piperidinyl)-N-phenylamides

Novel N-(4-piperidinyl)-N-phenylamides and -carbamates having very potent analgesic activity, methods of preparing same and useful intermediates therefor.

N-(4-piperidinyl)-N-phenylamides and -carbamates

Novel N-(4-piperidinyl)-N-phenylamides and -carbamates having very potent analgesic activity, methods of preparing same and useful intermediates therefor.