HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012182Generated: October 30, 2026
2-Pyridinecarboxaldehyde → HCID 59468437, compound
https://huagongshe.com/reaction/1012182
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Pyridinecarboxaldehyde | HCID 14273 | — |
| Reactant | HCID 59468418 | HCID 59468418 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 59468437 | HCID 59468437 | — |
Reaction Steps
A solution of [4-(5-aminothiophen-2-yl)-pyrimidin-2-yl]-m-tolyl-amine (prepared according to Method 4) (15 mg, 0.053 mmol) and pyridine-2-carbaldehyde (4.5 uL, 0.048 mmol) were dissolved in a 25% solution of HOAc in DMA (0.5 mL). MP-CNBH3 resin (2.5 eq.) was added after 2 h and the reaction was shaken for 18 h. The reaction was filtered and the resin washed with DMA. The crude mixture was purified by preparative LCMS to afford 11.1 mg, 61.2%). MS: m/z 374 (M+H+). 1H NMR (500 MHz, DMSO-d6) δ 2.26 (s, 3H), 4.42 (d, J=6.5 Hz, 2H), 5.96 (d, J=4.5 Hz, 1H), 6.72 (d, J=7.5 Hz, 1H), 6.986 (d, J=5.5 Hz, 1H), 7.10 (t, J=7.5 Hz, 1H), 7.27 (m, 1H), 7.38 (d, J=7.5 Hz, 1H), 7.47 (d, J=7.5 Hz, 1H), 7.56 (d, J=4.0 Hz, 1H), 7.73 (br s, 1H), 7.76 (m, 1H), 7.81 (t, J=5.5 Hz, 1H), 8.16 (d, J=6.0 Hz, 1H), 8.53 (br dd, J=4.5 Hz, 1H), 9.24 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977481B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-2f2c28727cbc4b6d90719c6aa82160b9 |
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| Source note | uspto-grants-2011_07 |
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