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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377579Generated: October 30, 2026

Methanol → HCID 10710154, compound

https://huagongshe.com/reaction/377579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantGuanidineHCID 3520—
ReactantGuanidine HydrochlorideHCID 5742—
ReactantSodiumHCID 5360545—
ReactantHCID 10729478HCID 10729478—
ProductHCID 10710154HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06028069
Source datasetuspto-grants-2000_02
ORD IDord-8d14de6095db40548175f013aba8b80d
Source noteuspto-grants-2000_02