4594-82-5

Upstream product

• 533-37-9 2,3-cyclopentenopyridine 
• 7148-07-4 1-pyrrolidinocyclopent-1-ene 
• 55618-82-1 2,4-dihydroxy-6,7-dihydro-5H-[1]pyrindine-3-carboxylic acid ethyl ester 
• 82297-48-1 1,3,4,5,6,7-Hexahydro-[1]pyrindine-2-thione 
• 10333-13-8 1Δ^4a(7a)-hexahydro-2(1H)-pyrindone 
• 4594-79-0 3,4,4a,5,6,7-hexahydro-2H-cyclopentapyridine 
• 1335288-25-9 1-benzenesulfonyl-2,3,7,7a-tetrahydro-1H-[1]pyridine 
• 1335288-18-0 6-allyl-1-benzenesulfonyl-5-vinyl-1,2,3,6-tetrahydropyridine 
• 1335288-34-0 C₁₆H₂₂BrNO₃S 
• 1335288-24-8 methanesulfonic acid 2-(2-allyl-1-benzenesulfonyl-3-bromo-piperidin-3-yl)-ethyl ester 
• 1335288-19-1 (2-allyl-1-benzenesulfonyl-3-bromo-piperidin-3-yl)-acetic acid ethyl ester 
• 1268245-93-7 (1-benzenesulfonyl-1,4,5,6-tetrahydro-pyridin-3-yl)-acetic acid ethyl ester 
• 611-10-9 2-ethoxycarbonyl-1-cyclopentanone 
• 7149-18-0 ethyl 2-amino-1-cyclopentene-1-carboxylate 

Relevant academic research and scientific papers

Enantioselective Hydroazidation of Trisubstituted Non-Activated Alkenes

A one-pot procedure for the enantioselective hydroazidation of non-activated trisubstituted alkenes is described. Hydroboration with monoisopinocampheylborane (IpcBH2) provides dialkylboranes that are in situ selectively converted into monoalkyl-substituted catecholboranes; these undergo radical azidation upon treatment with benzenesulfonyl azide and a radical initiator. Enantiomerically enriched azides were thus obtained in yields of 59–81 % and enantioselectivities of up to 94:6 e.r. (98:2 e.r. if the intermediate dialkylborane is purified by crystallization). A rapid access to enantiomerically pure (+)-rodocaine is also described. The use of other arenesulfonyl radical traps enables enantioselective hydroallylation, hydrosulfanylation, and hydrobromination reactions with yields of 71–86 %.

Synthesis of rodocaine

A new method for synthesis of rodocaine (1) is presented. Two key steps were carried out by the N-bromosuccinimide (NBS)-mediated intermolecular addition of known enamine 5 with allyltrimethyl silane in presence of boron trifluoride etherate (BF3/OEt2) and the intramolecular ring-closing metathesis of triene 3. The Diels-Alder cycloaddition of triene 3 with different ethyl propiolates was also studied.

Diastereoselective access to trans -2-substituted cyclopentylamines

A highly diastereoselective synthesis of trans-2-substituted cyclopentylamines via a tandem hydrozirconation/Lewis acid-mediated cyclization sequence applied to butenyl oxazolidines is described. The method allows an easy preparation of diversely substituted cyclopentylamines which appear to be useful synthetic intermediates. This was further illustrated by the syntheses of (±)-Rodocaine, (±)-trans-pentacin, and enantiomerically enriched trans-cyclopentane-1,2-diamine.

A Stereoselective Synthesis of (+/-)-trans-Cycloalkanopiperidines and Cycloalkanopyrrolidines via Hydroboration

A highly stereoselective synthesis of trans-cycloalkanopiperidines and cycloalkanopyrrolidines has been achieved via hydroboration of bromocycloalkenes with dichloroboranes.The intermediate bromocycloalkylboronic acids were converted into azidocycloalkylboronates.Addition of two equivalents of boron trichloride in dichloromethane generated dichloroboranes which, by an intramolecular cyclisation gave intermediates 11.These can be readily hydrolyzed to get the corresponding important nitrogen heterocycles in good yields and excellent stereochemical purities.

ENAMINE CHEMISTRY-XXIV. SYNTHESIS, THIATION, AND REDUCTION OF LACTAMS

Enamines, 1, prepared from cyclohexanones or cyclopentanones are reacted with acrylamide to give lactams, the condensed 2-piperidones, 2.Ethyl 2-(1-pyrrolidinyl)-2-cyclohexene-1-propanoate, 3, when treated with primary amines, produces the corresponding N-substituted 2-piperidones, 4.Ethyl 2-(1-pyrrolidinyl)-2-cyclohexene-1-ethanoates and ethyl 2-(1-pyrrolidinyl)-2-cyclopentene-1-ethanoate, 5, react with primary amines to give condensed N-substituted 2-pyrrolidones, 6, and non-cyclic imines, 7.The starting enamines , 1, treated with 2-bromo acetamides only afford the N-alkylated compounds, 8 (2-pyrrolidino acetamides), and the regioselectivity of this reaction is rationalized in terms of the HSAB-principle.Compound 1 undergoes an exchange reaction (aminolysis) when reacted with primary amines to give the imines 9.Thiation of the lactams 2 and 6 with the Lawesson reagent (LR), affords the corresponding thiolactams, 10.Reduction of the lactams and thiolactams, 2, 6, and 10 by LAH gives the imines, 11, and the enamines, 16.Further reduction of 11 (LAH) affords the saturated amines, 15.The stereochemistry for the formation of 15 is discussed using the torsion angle notation and the principal of least torsional distortion.In a one-pot reaction using LAH-acetic anhydride the lactams, 2, and the thiolactams, 10, are transformed into the enamides, 14.Compound 14 was also obtained from 11 by direct acetylation with acetic anhydride in the presence of triethylamine.