HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633775Generated: October 30, 2026
2-Methylpropylenediamine → HCID 10268741, compound
https://huagongshe.com/reaction/1633775
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methylpropylenediamine | HCID 13128 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (Z)-5-fluoro-4-[1-iodo-3-oxo-3-(1H-pyrrol-2-yl)-propenyl]-1,3-dihydro-indol-2-one | HCID 10135347 | — |
| Product | HCID 10268741 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06504034B2 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-6c438c74c0164251888f7d5e29b910bb |
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| Source note | uspto-grants-2003_01 |
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