Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057979Generated: October 31, 2026

Sodium Carbonate → 6H-Pyrido(2,3-b)(1,4)benzodiazepin-6-one, 5,11-dihydro-11-((4-(3-methyl-2-butenyl)-1-piperazinyl)acetyl)-, dihydrochloride

https://huagongshe.com/reaction/2057979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant11-(Chloroacetyl)-5,11-dihydro-6H-pyrido(2,3-b)(1,4)benzodiazepin-6-oneHCID 120053—
Reactant1-(3-Methyl-but-2-enyl)-piperazineHCID 10441904—
SolventIsopropanolHCID 3776—
Product6H-Pyrido(2,3-b)(1,4)benzodiazepin-6-one, 5,11-dihydro-11-((4-(3-methyl-2-butenyl)-1-piperazinyl)acetyl)-, dihydrochlorideHCID 3053213—

Reaction Steps

8.62 gm of 11-chloroacetyl-5,11-dihydro-6H-pyrido[2,3-b][1,4]-benzodiazepin-6-one, 3.5 gm of sodium carbonate and 5.07 gm of 1-(3-methyl-but-2-enyl)-piperazine [R1 =--CH2 --CH=C(CH3)2 ] were refluxed in 100 ml of isopropanol for 2.5 hours. Then, the reaction mixture was suction-filtered while still hot, and the filtrate evaporated to a volume of 40 ml and cooled. The precipitated crystals were dissolved, while heating, in 100 ml of absolute ethanol, and the calculated quantity of concentrated hydrochloric acid was added. Upon cooling, the dihydrochloride crystallized out.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04213984
Source datasetuspto-grants-1980_07
ORD IDord-dd91e9e1335e47f69a9fe278c1c3353d
Source noteuspto-grants-1980_07