HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177289Generated: November 2, 2026
2-Amino-5-methylpyridine → HCID 66756004, compound
https://huagongshe.com/reaction/1177289
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Amino-5-methylpyridine | HCID 15348 | — |
| Reactant | Chlorodimethylaluminum | HCID 79147 | — |
| Reactant | HCID 66755846 | HCID 66755846 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 66756004 | HCID 66756004 | 80% |
Reaction Steps
2-Amino-5-methylpyridine (264 mg, 2.44 mmol) was dissolved in DCE (10 mL) at 0° C., then Al(CH3)2Cl (2.44 mL, 1M in hexanes) was added drop wise. After the addition, the ice-bath was removed, and the mixture was stirred for 30 minutes at room temperature. Ethyl 2-(difluoromethyl)-4-[4-(methylsulfonyl)phenoxy]-1-benzofuran-6-carboxylate (100 mg, 0.244 mmol) was added, and the stirring was continued for 14 h. The reaction was quenched with potassium sodium tartrate tetrahydrate (20% w/w) cautiously. The product was extracted with CHCl3, washed with brine and dried over MgSO4. The product was purified by reverse phase HPLC to give the title compound (92 mg, 80%) as a white solid. 1H NMR (400 MHz, CHLOROFORM-D) δ ppm 2.31 (s, 3 H) 3.08 (s, 3 H) 6.75 (t, J=53.94 Hz, 1 H) 6.98 (s, 1 H) 7.12-7.20 (m, 2 H) 7.51 (d, J=1.01 Hz, 1 H) 7.58 (dd, J=8.46, 2.15 Hz, 1 H) 7.91-7.96 (m, 2 H) 7.97 (s, 1 H) 8.11 (d, J=2.15 Hz, 1 H) 8.23 (d, J=8.46 Hz, 1 H) 8.54 (s, 1 H). LCMS m/z 473.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842713B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-f4d7f92961c14d388fe6ec1d2e5f6590 |
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| Source note | uspto-grants-2010_11 |
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