HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864775Generated: November 1, 2026
1-Pyrrolidineethanamine → HCID 68746920, compound
https://huagongshe.com/reaction/1864775
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Pyrrolidineethanamine | HCID 1344 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 86616466 | HCID 86616466 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68746920 | HCID 68746920 | 31.8% |
Reaction Steps
Sodium triacetoxyborohydride (530 g, 2.51 mmol) and then enough acetic acid to bring the pH to 5 were added to a solution of 5-(4-fluoro-3-formylphenyl)-1H-indole (200 mg, 0.84 mmol) and 1-(2-aminoethyl)pyrrolidine (191 mg, 1.67 mmol) in 15 mL of 1,2-dichloroethane. The mixture was stirred at ambient temperature overnight, and then it was diluted with dichloromethane, and neutralized with the careful addition of saturated sodium bicarbonate solution. The layers were separated and the aqueous phase extracted into dichloromethane. The combined organic phases were dried over magnesium sulfate, filtered and concentrated to leave the crude product. Chromatography (elution with methanol/dichloromethane) provided 90 mg of the title compound. LC/MS: Retention time, 0.34 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07625889B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-bc37002e401345ea8f9a1c2fe043c5e5 |
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| Source note | uspto-grants-2009_12 |
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