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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22472Generated: October 27, 2026

Dimethylformamide → (2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-methoxyiminoacetyl chloride

https://huagongshe.com/reaction/22472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-(methoxyimino)acetic acidHCID 10130412—
Solvent1,2-DimethoxyethaneHCID 8071—
Product(2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-methoxyiminoacetyl chlorideHCID 10198354—

Reaction Steps

In 50.0 ml of 1,2-dimethoxyethane (DME), 10.0 g of 2- (5-amino-1,2,4-thiadiazol-3-yl)-2(Z)-methoxyiminoacetic acid were stirred at -20° C., followed by the dropwise addition of a chlorinating reagent, which had been prepared beforehand by gradually adding 8.4 g of phosphorus oxychloride at 5° C. to a mixture of 20 ml of DME and 4.0 g of N,N-dimethylformamide (DMF) and then reacting them for 30 minutes. After they were reacted for 5 minutes, the reaction mixture was poured into 160 ml of ice water to precipitate crystals. The resulting crystals were collected by filtration, washed with 200 ml of ice water and then stirred for 30 minutes in 120 ml of n-hexane. After filtration, the resulting crystals were dried under reduced pressure, whereby the title compound was obtained. Yield: 8.43 g (76.6%). Purity: 97.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428173
Source datasetuspto-grants-1995_06
ORD IDord-0757c3bbfa1d443bb6f3447a86ec152b
Source noteuspto-grants-1995_06