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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473304Generated: November 1, 2026

3-Amino-5-methylisoxazole → 5-(4-chloro-2-methoxyphenyl)-N-(5-methylisoxazol-3-yl)naphthalene-2-sulfonamide

https://huagongshe.com/reaction/1473304

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-5-methylisoxazoleHCID 66172—
Reactant5-(4-Chloro-2-methoxyphenyl)naphthalene-2-sulfonyl chlorideHCID 86687361—
Product5-(4-chloro-2-methoxyphenyl)-N-(5-methylisoxazol-3-yl)naphthalene-2-sulfonamideHCID 8668736231,862.699%

Reaction Steps

This product was prepared as described in Example 43, employing 5-methylisoxazol-3-amine (48.0 mg, 0.49 mmol) and 5-(4-chloro-2-methoxyphenyl)naphthalene-2-sulfonyl chloride (0.498 μl, 0.408 μmol) to provide 5-(4-chloro-2-methoxyphenyl)-N-(5-methylisoxazol-3-yl)naphthalene-2-sulfonamide (55.8 mg, 0.13 mmol) as an off-white solid. 1H NMR (500 MHz, DMSO-d6) δ ppm 2.27 (s, 3H), 3.67 (s, 3H), 6.19 (s, 1H), 7.12-7.21 (m, 1H), 7.23-7.31 (m, 2H), 7.53-7.64 (m, 2H), 7.69-7.81 (m, 2H), 8.21 (d, J=8.30 Hz, 1H), 8.59 (d, J=1.78 Hz, 1H), 11.55 (br. s., 1H); m/z (ESI, +ve ion) 429.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012443B2
Source datasetuspto-grants-2015_04
ORD IDord-c6e36c7de1774d939b5be7fdf472706f
Source noteuspto-grants-2015_04