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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729943Generated: October 31, 2026

Tetrahydrofuran → HCID 21498439, compound

https://huagongshe.com/reaction/1729943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantN-MethylfurfurylamineHCID 78492—
ReactantHCID 13563611HCID 13563611—
SolventWaterHCID 962—
ProductHCID 21498439HCID 21498439—

Reaction Steps

To a solution of 8.4 g. of 2-methylamino-1,3,4-thiadiazole-5-sulfonyl chloride (see Preparation 1) in 100 ml. of tetrahydrofuran, cooled to about 0° C., there was added dropwise 4.4 g. of methylfurfurylamine. After the addition had been completed, 4.1 g. of triethylamine was added to the mixture dropwise and the mixture was then stirred at ambient room temperature overnight. The reaction product mixture was filtered to remove any salt. The filtrate was concentrated to yield an oil. Water was added to the oil. A precipitate formed which was filtered off and dried. The precipitate weighed about 6.2 g. and had a melting point of about 109°-112° C. It was identified as 2-methylamino-5-[N-methyl-N-furfurylsulfamoyl]-1,3,4-thiadiazole. It was used without further purification in the preparation of some of the final products of the invention.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03990881
Source datasetuspto-grants-1976_11
ORD IDord-2f737b30196742b8b5341176459dfd22
Source noteuspto-grants-1976_11