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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247570Generated: October 31, 2026

Dimethylformamide → HCID 20159873, compound

https://huagongshe.com/reaction/247570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPhenacyl bromideHCID 6259—
Reactant2-Amino-5-bromo-1,3,4-thiadiazoleHCID 3650883—
ProductHCID 20159873HCID 20159873—

Reaction Steps

18.0 g of 2-bromo-5-amino-1,3,4-thiadiazole (0.1 mol) and 20.0 g of ω-bromoacetophenone (0.1 mol) in 250 ml of dimethylformamide are heated to 100° C. for 4.5 hours. After cooling down to room temperature, 100 ml of icewater are added and the precipitate is filtered off with suction. After drying, it is taken up in chloroform and, after the addition of ether, recrystallized. The crude 2-bromo-6-phenylimidazo[2,1-b]-1,3,4-thiadiazole is then heated to reflux for 2 hours in 250 ml of ethanol with 25 ml of 30% strength methylamine solution. After cooling down, precipitation is by addition of 200 ml of water, the precipitate is filtered off with suction and recrystallized from chloroform/ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04709031
Source datasetuspto-grants-1987_11
ORD IDord-880c5c5d9abf4bc9a28c7c7b1aa56962
Source noteuspto-grants-1987_11