18807-70-0

Upstream product

• 462-94-2 1,5-diaminopentane 
• 501-53-1 benzyl chloroformate 
• 34237-69-9 N,N'-di-(tert-butoxycarbonyl)-1,5-diaminopentane 
• 100-51-6 benzyl alcohol 

Downstream Products

• 70034-25-2 N-(2,4-dinitro-phenyl)-pentanediyldiamine 
• 113431-67-7 [5-(2,4-dinitro-anilino)-pentyl]-carbamic acid benzyl ester 
• 69747-37-1 {5-[3-(5-Benzyloxycarbonylamino-pentyl)-thioureido]-pentyl}-carbamic acid benzyl ester 
• 89450-71-5 N-<3-(1-uracilyl)propyl>-N'-carbobenzoxypentamethylenediamine hydrobromide 
• 89450-67-9 N-<2-(1-uracilyl)ethyl>-N'-carbobenzoxypentamethylenediamine hydrobromide 
• 18807-74-4 N-benzyloxycarbonyl-1,5-pentanediamine hydrochloride 
• 73429-15-9 6,7,10,11,12,13,15,16-octahydro-9H-5,17-dioxa-8,14-diaza-dibenzo[a,c]cycloheptadecene-8,14-dicarboxylic acid dibenzyl ester 
• 69747-36-0 (5-aminopentyl)carbamic acid benzyl ester 

Relevant academic research and scientific papers

Convenient protection of amines as carbamates using polymer-bound HOBT as catalyst

A method for the facile protection of primary and secondary amines as carbamate (Cbz, Fmoc and t-Boc) derivatives using polymer bound 1-hydroxybenzotriazole (HOBT) is reported.

Renin inhibitors containing 5-amino-2,5-disubstituted-4-hydroxypentanoic acid residues

A series of novel polypeptide derivatives, containing 5-amino-2,5-disubstituted-4-hydroxypentanoic acid residues, which are useful for inhibiting the angiotensinogen-cleaving action of the enzyme renin. Particularly valuable precursors for many of these compounds are certain other 5-amino-2,5-disubstituted-4-hydroxypentanoic acid derivatives.

SYNTHESIS OF N-(1-URACILYLALKYL)POLYMETHYLENEDIAMINES

The alkylation of polymethylenediamines with 2-(1-uracilyl)ethyl bromide and 3-(1-uracilyl)propyl bromide yields the corresponding N-(1-uracilylalkyl)polymethylendiamines.