HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 10710154, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Guanidine | HCID 3520 | — |
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 10729478 | HCID 10729478 | — |
| Product | HCID 10710154 | HCID 10710154 | — |
Reaction Steps
A guanidine solution prepared--as described in Example 3--from 547 mg of sodium, 12 ml of methanol and 2.5 g of guanidine hydrochloride is treated with 1.2 g of methyl 2,3-dihydro-5-methyl-3-methylene-1-benzothiophene-6-carboxylate-1,1-dioxide [prepared by cyclization of methyl 4-acetyl-2-methyl-5-methylsulfonylbenzoate and subsequent dehydration] and the mixture is boiled for 1 hour, then stirred at room temperature for a further hour and worked up in the customary manner. N-Diaminomethylene-2,3-dihydro-3-methoxy-3,5-dimethyl-1-benzothiophene-6-carboxamide-1,1-dioxide is obtained. Treatment with methanesulfonic acid in methanol gives the corresponding methanesulfonate, m.p. 214-215°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06028069 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-8d14de6095db40548175f013aba8b80d |
| Source note | uspto-grants-2000_02 |