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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526694Generated: November 2, 2026

Dimethylamine, hydrochloride → HCID 56644018, compound

https://huagongshe.com/reaction/1526694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86679716HCID 86679716—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 56644018HCID 56644018—

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) (75 mg) was dissolved in DCM (5 ml). Dimethylamine hydrochloride (18.42 mg) and acetic acid (8.62 μl) were added and the reaction mixture was stirred for 5 min. Sodium triacetoxyborohydride (160 mg) was added and the reaction mixture was stirred at room temperature, under nitrogen, for 5 h. 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 overnight to give (S)-2-(6-(4-chlorophenyl)-8-(4-((dimethylamino)methyl)phenyl)-1-methyl-4H-benzo[f][1,2,4]triazolo[4,3-a][1,4]diazepin-4-yl)-N-ethylacetamide (48.2 mg) as a white solid. LCMS (formate): MH+ 527/529, RT 0.66 min

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085582B2
Source datasetuspto-grants-2015_07
ORD IDord-9b39d08f5cd2455ca7267840f60416b5
Source noteuspto-grants-2015_07