HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxane → 4-Amino-3-methylisothiazole-5-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 4-((tert-Butoxycarbonyl)amino)-3-methylisothiazole-5-carboxylic acid | HCID 54757214 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 4-Amino-3-methylisothiazole-5-carboxylic acid | HCID 22831852 | — |
Reaction Steps
4-tert-Butoxycarbonylamino-3-methyl-isothiazole-5-carboxylic acid (method 56) (11 g, 45 mmol) was dissolved in 50 mL of 4M solution of HCl in 1,4-dioxane (200 mmol) and the resulting solution was stirred at room temperature overnight. The TLC showed the complete disappearance of the starting acid. The reaction was concentrated and the residue was triturated with ether and the precipitated hydrochloride salt was filtered off and washed with ether and dried to provide the product as a light brown powder. Yield 8.2 g (100%). 1H NMR (300 MHz, DMSO-d6) δ 2.30 (s, 3H), 8.85 (bs, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07498333B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-e7dc112e99194e489a6f48d4466c973a |
| Source note | uspto-grants-2009_03 |