Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633775Generated: October 30, 2026

2-Methylpropylenediamine → HCID 10268741, compound

https://huagongshe.com/reaction/1633775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylpropylenediamineHCID 13128—
ReactantSodium hydrideHCID 24758—
Reactant(Z)-5-fluoro-4-[1-iodo-3-oxo-3-(1H-pyrrol-2-yl)-propenyl]-1,3-dihydro-indol-2-oneHCID 10135347—
ProductHCID 10268741HCID 10268741—

Reaction Steps

To a suspension of (Z)-5-fluoro-4-[1-iodo-3-oxo-3-(1H-pyrrol-2-yl)-propenyl]-1,3-dihydro-indol-2-one (from Example 8 above) (79.2 mg, 0.2 mmol) in 1,2-diamino-2-methylpropane (Aldrich, 3 mL, 28.4 mmol) was added NaH (Aldrich, 90%, 36 mg, 1.4 mmol) in portions at room temperature. After stirring at room temperature for 30 minutes, the reaction mixture was heated under reflux for 1 hour. The reaction was quenched by pouring the reaction mixture into an ice-cold saturated aqueous ammonium chloride solution (10 mL) and extracted with ethyl acetate (3×20 mL). The combined organic extracts were successively washed with water (10 mL) and brine (10 mL), dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The crude product was purified by preparative TLC (silica gel, 5% methanol in ethyl acetate) to afford 5-(2-amino-2-methyl-propylamino)-6-fluoro-3-(1H-pyrrol-2-yl)-1H-benzo[cd]indol-2-one as a brown solid. (Yield 4.4 mg, 6.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06504034B2
Source datasetuspto-grants-2003_01
ORD IDord-6c438c74c0164251888f7d5e29b910bb
Source noteuspto-grants-2003_01