HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75764Generated: October 28, 2026
Methyl iodide → HCID 178501506, compound
https://huagongshe.com/reaction/75764
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | (S)-2-({3-[4-(6-fluoro-benzothiazol-2-ylamino)-phenyl]-isoxazole-5-carbothioyl}-amino)3-methyl-butyric acid methyl ester | HCID 46181830 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178501506 | HCID 178501506 | 68% |
Reaction Steps
To a solution of freshly cleaned sodium pieces (0.043 g; 1.86 matom) in dry MeOH (30 ml) was added (S)-2-({3-[4-(6-fluoro-benzothiazol-2-ylamino)-phenyl]-isoxazole-5-carbothioyl}-amino)3-methyl-butyric acid methyl ester (0.9 g; 1.86 mmol) under stirring followed by iodomethane (0.23 ml; 3.72 mmol). The stirring was continued for 2 hours at room temperature. Hydroxylamine hydrochloride (0.284 g; 4.09 mmol) was added to this solution followed by NaHCO3 (0.343 g; 4.09 mmol) and the resulting reaction mixture was refluxed for 3 hours. The solid thus obtained was filtered, dried and purified by flash chromatography over silica gel with 5% MeOH in chloroform to obtain 0.61 g (68%) of the title compound. Mass (ES−): 482 (M−1); IR (KBr): 3384, 3196, 2963, 1737, 1642, 1611, 1546 (br), 1462 (br); 1H NMR (DMSO-d6) δ: 0.89, 0.94 (2×d, 6H), 2.08 (m, 1H), 3.65 (s, 3H), 3.99 (m, 1H), 5.85 (d, 1H), 7.20 (m, 1H), 7.29 (s, 1H), 7.66 (m, 1H), 7.79 (m, 1H), 7.93 (s, 4H), 10.78 (s, 1H); 10.85 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835428B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-0a3a1299eb51407fa2f94d490aed4ba9 |
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| Source note | uspto-grants-2014_09 |
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