HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600173Generated: November 1, 2026
3-Pyridinecarboxaldehyde → HCID 10881145, compound
https://huagongshe.com/reaction/1600173
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | 5-Bromo-2-methylindole | HCID 5003968 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 10881145 | HCID 10881145 | 75% |
Reaction Steps
A solution of 5-bromo-2-methyl-1H-indole (J. Chem. Soc., 1428 (1965)) (2.0 g) and 3-pyridinecarboxaldehyde (1.02 g) in dry dichloromethane (20 ml) was added dropwise over 10 minutes to a stirred solution of triethylsilane(3.30 g) in trifluoroacetic acid (20 ml) at 0° C. The solution was stirred at 0° C. for 30 minutes and then evaporated under vacuum, keeping the temperature below 35° C. The residue was dissolved in dichloromethane, and the solution was washed with 2N sodium hydroxide, water and dried (MgSO4). The solution was evaporated and the residue was chromatographed on silica gel, using dichloromethane/methanol (50:1) as eluent. The product fractions were combined and evaporated, and the residue was crystallised from ether to give the title compound (2.15 g), m.p. 188°-190° C. Found: C,59.62; H,4.43; N,9.26. C15 H13BrN2 requires: C,59.82; H,4.35; N,9.30%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05744488 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-75f2916e50af49b79d8f15e75eef7ee4 |
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| Source note | uspto-grants-1998_04 |
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