Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418901Generated: October 31, 2026

Dipropylamine → HCID 18392572, compound

https://huagongshe.com/reaction/1418901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDipropylamineHCID 8902—
ReactantN-IodosuccinimideHCID 120273—
ReactantHCID 86753941HCID 86753941—
SolventAcetic AcidHCID 176—
ProductHCID 18392572HCID 1839257228%

Reaction Steps

A solution of 3.30 g (0.0098 mol) of (S)-8-chloro-9-oxo-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepine-1-carboxylic acid prop-2-ynylamide in 60 mi of acetic acid was treated with 3.30 g (0.0147 mol) of N-iodosuccinimide while gassing with argon. After stirring at room temperature for 24 hrs. the dark brown suspension obtained was completely freed from the solvents and dried azeotropically several times with toluene. The dark viscous residue was dissolved in 60 ml of THF, treated with 11.9 ml (0.0865 mol) of dipropylamine and stirred at room temperature for 24 hrs. The suspension obtained was filtered and the solution was completely freed from the solvents, the residue was partitioned between ethyl acetate and dilute aqueous hydrochloric acid and extracted. The aqueous-acidic phase was made basic and extracted with ethyl acetate. The organic phase was concentrated and the residue was chromatographed over silica gel with dichloromethane/methanol 98:2 as the eluent. There were obtained 1.19 g (28%) of (S)-8-chloro-1-(5-dipropylaminomethyl-oxazol-2-yl)-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepin-9-one as yellow crystals; m.p. 148°-151° (dec.) and [α]D20 =-101.7° (MeOH, c=1%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05885986
Source datasetuspto-grants-1999_03
ORD IDord-8e699790a7c7401d886ce3fbb2b0680c
Source noteuspto-grants-1999_03