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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530792Generated: October 28, 2026

Chlorosuccinimide → HCID 90419267, compound

https://huagongshe.com/reaction/530792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 90454510HCID 90454510—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 90419267HCID 90419267—

Reaction Steps

To a solution of 4-((1,3-dimethyl-1H-pyrazol-5-yl)methylamino)-2-methyl-6-(((1S,2S)-2-(5-methylpyridin-2-yl)cyclopropyl)methoxy)pyridazin-3(2H)-one (10 mg, 0.025 mmol) in 1,2-Dichloroethane (2.0 mL) was added NCS (4.0 mg, 0.030 mmol). After stirred for 1 h at rt, the reaction mixture was concentrated. The residue was purified by reverse phase chromatography (X bridge Prep C18OBD, 40-60% acetonitrile in water with 10 mmol NH4HCO3 modifier) to obtain product. 1H NMR (400 MHz, MeOD) δ 8.21 (s, 1H), 7.53 (d, 1H), 7.14 (d, 1H), 5.91 (s, 1H), 4.42 (s, 2H), 4.21-4.16 (m, 1H), 4.11-4.06 (m, 1H), 3.79 (s, 3H), 3.63 (s, 3H), 2.31 (s, 3H), 2.19 (s, 3H), 2.12-2.06 (m, 1H), 1.82-1.79 (m, 1H), 1.25-1.20 (m, 1H), 1.10-1.05 (m, 1H); LRMS m/z (M+H) 429.1 found, 429.17 required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353104B2
Source datasetuspto-grants-2016_05
ORD IDord-37199815ffa54a35b498b8e3e77747f9
Source noteuspto-grants-2016_05