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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526689Generated: November 4, 2026

Ethylamine hydrochloride → HCID 56643812, compound

https://huagongshe.com/reaction/1526689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamine hydrochlorideHCID 11198—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86679714HCID 86679714—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 56643812HCID 56643812—

Reaction Steps

(S)-2-(6-(4-Chlorophenyl)-8-(3-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 5) (75 mg) was dissolved in DCM (5 ml). Ethylamine 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, overnight. 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) and triturated with diethyl ether. The solid was dried in a vacuum dessicator at 40° C. over the weekend to give (S)-2-(6-(4-chlorophenyl)-8-(3-((ethylamino)methyl)phenyl)-1-methyl-4H-benzo[f][1,2,4]triazolo[4,3-a][1,4]diazepin-4-yl)-N-ethylacetamide (52.4 mg) as a white solid. LCMS (formate): MH+ 527, RT 0.75 min

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085582B2
Source datasetuspto-grants-2015_07
ORD IDord-db0cc25bb72743bb988daa936336432f
Source noteuspto-grants-2015_07