HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295448Generated: October 26, 2026
Dimethylformamide → 2-Aminoquinoline-6-carbaldehyde
https://huagongshe.com/reaction/1295448
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | CID 76231 | HCID 76231 | — |
| Reactant | Diphenylpropyl phosphine | HCID 53436545 | — |
| Reactant | HCID 58907866 | HCID 58907866 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | 2-Aminoquinoline-6-carbaldehyde | HCID 22018906 | 24% |
Reaction Steps
A mixture of 6-iodo-quinolin-2-ylamine (200 mg, 0.74 mmol), triethylamine (0.26 mL, 1.85 mmol), diphenylpropylphosphine (dpp, 17 uL, 0.074 mmol) and palladium(II) acetate (17 mg, 0.074 mmol) in dry N,N-dimethylformamide (4 mL) in pressure tube was stirred under carbon monoxide at 75 psi at room temperature for 10 min. After addition of trihexylsilane (0.53 mL, 1.5 mmol), the mixture was then stirred under carbon monoxide at 75 psi at 80° C. for 4 h. The reaction was allowed to cool to 25[ ]C and then extracted with methylene chloride (2×50 mL). The combined organic layers were successively washed with water (3×50 mL), dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 70–230 mesh, ethyl acetate) afforded 2-amino-quinoline-6-carbaldehyde (30 mg, 24%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07241893B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-7e0497d3457b4dd1916693b1caee48d4 |
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| Source note | uspto-grants-2007_07 |
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