HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520105Generated: October 29, 2026
Triethylamine → [4-[6-(Aminomethyl)-2-methyl-pyrimidin-4-yl]oxyphenyl]methanesulfonamide
https://huagongshe.com/reaction/1520105
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | [4-(6-Cyano-2-methyl-pyrimidin-4-yl)oxyphenyl]methanesulfonamide | HCID 118093606 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | [4-[6-(Aminomethyl)-2-methyl-pyrimidin-4-yl]oxyphenyl]methanesulfonamide | HCID 118093607 | 77% |
Reaction Steps
Combine triethylamine (117.83 mL) and palladium 10% on charcoal (20.10 g) to a solution of [4-(6-cyano-2-methyl-pyrimidin-4-yl)oxyphenyl]methanesulfonamide (67 g, 211.35 mmoles) in a mixture of 1,4-dioxane (469 mL) and EtOH (201 mL; 159.05 g) in a PARR reactor. Maintain the mixture at 22° C. Seal the reactor and pressurize it with hydrogen (400 PSI). Shake the reactor for 18 h while maintaining it at 22° C. Thereafter open the reactor and filter of the solids. Rinse the solid residue with MeOH (1 L), a mixture of dioxane/MeOH 1:1 (1 L), and MeOH (3×1 L). Collect and concentrate the filtrate to provide a solid, Collect and dry the solid in a vacuum oven, (45° C., 15 mbar) to provide the title compound as yellow solid, 62.41 g, 77% yield. MS (m/z): 309 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073901B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-7e2dc601304d4811a8a7066620a159eb |
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| Source note | uspto-grants-2015_07 |
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