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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351426Generated: November 3, 2026

Ammonia → 5,11-Dihydro-11-[[[2-[4-[3-(dipropylamino)propyl]-piperidin-1-yl]ethyl]amino]carbonyl]-9-methyl-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one

https://huagongshe.com/reaction/2351426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant11-(chlorocarbonyl)-5,11-dihydro-9-methyl-6H-pyrido[2,3-b][1,4]benzodiazepin-6-oneHCID 15107471—
Reactant2-[4-[3-(Dipropylamino)propyl]-piperidin-1-yl]ethanamineHCID 19846011—
SolventDichloromethane cyclohexane methanolHCID 69163855—
Product5,11-Dihydro-11-[[[2-[4-[3-(dipropylamino)propyl]-piperidin-1-yl]ethyl]amino]carbonyl]-9-methyl-6H-pyrido[2,3-b][1,4]benzodiazepin-6-oneHCID 1984594863%

Reaction Steps

Prepared analogously to Example 1 from 11-(chlorocarbonyl)-5,11-dihydro-9-methyl-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one and 2-[4-[3-(dipropylamino)propyl]-piperidin-1-yl]ethanamine in a yield of 63% of theory. Colourless crystals, m.p. 195° C. (D.), RF =0.5 (Macherey-Nagel, Polygram® SIL G UV254, pre-coated plastic sheets for TLC, eluant: dichloromethane/cyclohexane/methanol/conc. ammonia 68/15/15/15/2 v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873236
Source datasetuspto-grants-1989_10
ORD IDord-c4c45fdccaa844499c1de97ccbca122e
Source noteuspto-grants-1989_10