HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542688Generated: October 26, 2026
Water → N-[(4-Methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-1,4-benzodioxan-5-sulfonamide
https://huagongshe.com/reaction/542688
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Methyl (4-methoxy-6-methylpyrimidin-2-yl)carbamate | HCID 13072161 | — |
| Reactant | 2,3-Dihydro-1,4-benzodioxine-5-sulfonamide | HCID 13455428 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[(4-Methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]-1,4-benzodioxan-5-sulfonamide | HCID 13455430 | — |
Reaction Steps
To a solution of 1.0 g 1,4-benzodioxan-5-sulfonamide, prepared in Example 15, in 50 ml methylene chloride at ambient temperature under nitrogen was added 2.5 ml trimethylaluminum (2M in toluene). After stirring 15 minutes at ambient temperature, 1.0 g of methyl[4-methoxy-6-methylpyrimidin-2-yl]carbamate, prepared according to the procedure of Example 3, was added and the reaction mixture was heated at reflux for 72 hours. The reaction mixture was cooled to ambient temperature and 75 ml water, 10 ml glacial acetic acid and 10 drops hydrochloric acid were sequentially added. The organic phase was separated, dried, and the solvent removed under reduced pressure to give an oil. Crystallization of the oil from n-butyl chloride/ether gave a solid, m.p. 203°-205° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04659368 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-28d558f51c7d45fb9884936b786897c0 |
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| Source note | uspto-grants-1987_04 |
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