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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631896Generated: October 30, 2026

Dichloromethane → HCID 24771573, compound

https://huagongshe.com/reaction/631896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-IsopropylpiperazineHCID 78013—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Bromopyridine-2-carboxylic acidHCID 593919—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 57425298HCID 57425298—
SolventWaterHCID 962—
ProductHCID 24771573HCID 2477157354%

Reaction Steps

(6-Bromo-pyridin-2-yl)-(4-isopropyl-piperazin-1-yl)-methanone. To a solution of 6-bromo-pyridine-2-carboxylic acid (100.00 mg, 0.50 mmol) in DCM (5.0 mL) was added 1-isopropylpiperazine (95.20 mg, 0.74 mmol) followed by 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC; 189.78 mg, 0.99 mmol), 1-hydroxybenzotriazole (HOBt; 133.78 mg, 0.99 mmol), and iPr2NEt (0.86 mL, 4.95 mmol). After 18 h at rt, the mixture was diluted with water and extracted with DCM. Purification by FCC provided the desired product (83.0 mg, 54%). MS (ESI): mass calcd. for C13H18BrN3O, 311.06; m/z found, 312.2 [M+H]+. 1H NMR (CDCl3): 7.69-7.59 (m, 2H), 7.56-7.52 (m, 1H), 3.84-3.76 (m, 2H), 2.79-2.68 (m, 1H), 2.62 (t, J=5.1 Hz, 2H), 2.53 (t, J=5.1 Hz, 2H), 1.06 (d, J=6.5 Hz, 6H). Assay 1 (Human H3): Ki=1400 nM.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321729B2
Source datasetuspto-grants-2016_04
ORD IDord-8516f151b2da42379e7d3f4d2e0c7f98
Source noteuspto-grants-2016_04