Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526692Generated: November 3, 2026

1-Methylpiperazine → HCID 56644017, compound

https://huagongshe.com/reaction/1526692

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86679716HCID 86679716—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 56644017HCID 56644017—

Reaction Steps

(S)-2-(6-(4-Chlorophenyl)-8-(4-formylphenyl)-1-methyl-4H-benzo[f][1,2,4]triazolo[4,3-a][1,4]diazepin-4-yl)-N-ethylacetamide (for a preparation see Intermediate 6) (90 mg) was dissolved in DCM (5 ml). 1-Methylpiperazine (30 μl) and acetic acid (10.35 μl) were added and the reaction mixture was stirred for 5 min. Sodium triacetoxyborohydride (192 mg) was added and the reaction mixture was stirred at room temperature, under nitrogen, over the weekend. Saturated sodium hydrogen carbonate solution (5 ml) was added and the reaction mixture was stirred for 10 min. The organic phase was separated and the saturated sodium hydrogen carbonate solution was extracted with DCM (10 ml). The DCM extracts were combined, dried and the solvent was evaporated. The residue was chromatographed (0-15% methanol:DCM), triturated with diethyl ether and dried in a vacuum dessicator at 40° C. overnight to give (S)-2-(6-(4-chlorophenyl)-1-methyl-8-(4-((4-methylpiperazin-1-yl)methyl)phenyl)-4H-benzo[f][1,2,4]triazolo[4,3-a][1,4]diazepin-4-yl)-N-ethylacetamide (66.5 mg) as a white solid. LCMS (formate): MH+ 582, RT 0.65 min

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085582B2
Source datasetuspto-grants-2015_07
ORD IDord-e5aef58aaa3b41bb9abc215830a0d1cb
Source noteuspto-grants-2015_07