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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703879Generated: October 30, 2026

Bromo-4'-chloro-3'-sulfamoylacetophenone → HCID 22760495, compound

https://huagongshe.com/reaction/1703879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromo-4'-chloro-3'-sulfamoylacetophenoneHCID 12952390—
ReactantHCID 19686552HCID 19686552—
SolventDiethyl EtherHCID 3283—
ProductHCID 22760495HCID 22760495—

Reaction Steps

4.7 g of 2-bromo-4'-chloro-3'-sulfamoylacetophenone and 3 g of 1-ethyl-3-(2-pyridylmethyl)-thiourea were reacted according to the prescription given in Example 23 and 150 ml of diethyl ether were added to the reaction mixture. The hygroscopic 3-ethyl-4-(4-chloro-3-sulfamoylphenyl)-2-(2-pyridylmethylimino)-1,3-thiazolidine-4-ol-hydrobromide which had separated as crystals was rapidly filtered off, dissolved in 50 ml of water and converted into the end product as described in Example 28. Colorless solid body, decomposition beginning at 135° C., γC=N 1615 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04125614
Source datasetuspto-grants-1978_11
ORD IDord-11be9a6f3f534fceba4d4e2707ad6e9e
Source noteuspto-grants-1978_11