HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13371034, compound → HCID 70410313, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13371034 | HCID 13371034 | — |
| Reactant | methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide | HCID 54676532 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 70410313 | HCID 70410313 | 22.3% |
Reaction Steps
A mixture of 0.52 g (4 mmole) of 5-(methoxymethyl)-3-isoxazolamine, 1.08 g (4 mmole) of methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide, and 100 ml of xylene is heated at reflux for six hours in a soxhlet apparatus, the thimble of which contains 20 g of Linde type 4A molecular sieve. The reaction mixture is filtered to clarify it and is allowed to stand at room temperature overnight when the product crystallizes out. The product is filtered, washed with methanol-ether mixture, and then recrystallized from methanol to give 0.326 g of white crystals, mp 218°-223° C. dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04581458 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-38491a61eb7a48999c4aa4c65b76a891 |
| Source note | uspto-grants-1986_04 |