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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350432Generated: October 31, 2026

N-methyl-2-pyrrolidone → HCID 136005594, compound

https://huagongshe.com/reaction/1350432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantHCID 58860736HCID 58860736—
ReactantOlanzamineHCID 135446208—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 136005594HCID 13600559434.2%

Reaction Steps

Combine (S)-2-(2-naphthalen-2-yl-ethyl)-piperazine (854 mg, 3.72 mmol), 2-methyl-4H-3-thia-4,9-diaza-benzo[f]azulen-10-ylamine (895 mg, 3.72 mmol) and 1-methyl-2-pyrrolidinone (8 mL). Heat at reflux. After 5 h, cool to ambient temperature and dilute with ethyl acetate and water. Extract with ethyl acetate. Wash the extracts with water and brine, dry over sodium sulfate, filter and concentrate the filtrate. Purify by silica gel chromatography using 2N ammonia in methanol-methylene chloride (2.5%) as the eluent to give 576 mg (34%) of the title compound: mass spectrum (ion spray): m/z=453 (M+1), 451 (M−1). HR-MS calculated for C28H29N4S: 453.2113. Found 453.2116. HPLC: Symmetry C18 column (3.5 μm, 4.6×50 mm). Gradient 5% to 90% solvent B in 7 min. Solvent A was 0.1% (v/v) TFA in water and solvent B was acetonitrile. Retention time 5.7 min; 100% pure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214673B2
Source datasetuspto-grants-2007_05
ORD IDord-8cd8a5b4d339440a84037450a617baf4
Source noteuspto-grants-2007_05