HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071937Generated: October 27, 2026
4-amino-N-(2-methoxyethyl)benzene-1-sulfonamide → HCID 10110828, compound
https://huagongshe.com/reaction/1071937
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-amino-N-(2-methoxyethyl)benzene-1-sulfonamide | HCID 16781918 | — |
| Reactant | HCID 22390594 | HCID 22390594 | — |
| Solvent | (+-)-2-Butanol | HCID 6568 | — |
| Product | HCID 10110828 | HCID 10110828 | 77.2% |
Reaction Steps
2-Chloro-5-cyano-4-cyclopropylaminopyrimidine (Method 96; 295 mg, 1.28 mmol) was dissolved in hot 2-butanol (3 ml). A hot solution of 4-[N-(2-methoxyethyl)sulphamoyl]aniline (Method 5; 207 mg, 0.90 mmol) in 2-butanol (3 ml) was added and the reaction was stirred and heated at 90° C. for 1 hour. The reaction mixture was cooled and the volatiles evaporated to give a solid. The solid residue was triturated with hot ethyl acetate, cooled, and the resultant solid collected by filtration to give the title compound (270 mg, 77%). NMR: 0.68 (m, 2H), 0.80 (m, 2H), 2.88 (m, 3H), 3.14 (s, 3H), 3.28 (m, 2H), 7.48 (brs, 1H), 7.70 (d, 2H), 8.05 (d, 2H), 8.12 (brs, 1H) 8.41 (s, 1H), 10.31 (s, 1H); m/z: 389.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06908920B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-66a55060a6414b15985b012386beee66 |
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| Source note | uspto-grants-2005_06 |
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