HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966060Generated: October 31, 2026
2-Phenylindole-3-carboxaldehyde → HCID 178513138, compound
https://huagongshe.com/reaction/966060
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Phenylindole-3-carboxaldehyde | HCID 613305 | — |
| Reactant | HCID 178513185 | HCID 178513185 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178513138 | HCID 178513138 | 20% |
Reaction Steps
A mixture of DMF (11.0 mL, 142 mmol) and phosphorous oxychloride (3.63 mL, 39 mmol) is stirred at 0° C. for 1 h, a 0.2 mL portion is pipetted into a solution of 2-phenylindole (96 mg, 0.5 mmol) in DMF at 5° C. This reaction mixture is stirred at 5°-10° C. for 1 h, quenched with water, stored at −200 for 16 h and filtered. The filtercake is washed with water and dried in vacuo to afford the 2-phenylindole-3-carboxaldehyde intermediate. A suspension of the thus-obtained 2-phenylindole-3-carboxaldehyde (44.2 mg, 0.2 mmol) in isopropanol and concentrated HCl (50 μL) is treated with aminoguanidine bicarbonate (27 mg, 0.2 mmol), heated at 80° C. for 2 h, cooled to room temperature and concentrated in vacuo. The resultant residue is purified by HPLC to afford the title product, 28 mg (20% yield), identified by mass spectral and HPLC analyses (M+H) 277; retention time 3.76 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06951881B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-6ee6f18e123f46bfad902d60cc62044f |
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| Source note | uspto-grants-2005_10 |
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