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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107819Generated: November 1, 2026

Dimethylformamide → HCID 136114327, compound

https://huagongshe.com/reaction/2107819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHCID 14625407HCID 14625407—
CatalystZincHCID 23994—
SolventWaterHCID 962—
ProductHCID 136114327HCID 136114327—

Reaction Steps

A mixture of 2,3,4,5-tetrahydro-7-(methylthio)-3-phenyl-1H-[1,2,5]-triazepino[1,2-a][1,2,4]benzotriazine (0.5000 g), zinc dust (2.0 g), N,N-dimethylformamide (16 ml) and water (4 ml) was stirred magnetically and heated under reflux for 20 hours. The cooled mixture was filtered through Celite and the filter pad washed with N,N-dimethylformamide. The filtrate and washings were evaporated under oil pump vacuum to a syrup. The syrup was dissolved in dichloromethane and applied to the edges of 4 plates of Alox-100 uv254 (20×20 cm×1 mm). The plates were developed twice in dichloromethane and several times in chloroform. The major band was excised and the component eluted by stirring with methanol. The adsorbent was filtered and washed with methanol. The filtrate and washings were evaporated to a syrup. The syrup was extracted with dichloromethane and the solution was evaporated to a syrup which crystallized. The crystals were dissolved in dichloromethane and the solution was treated with charcoal and filtered through Celite. Evaporation gave a syrup which was crystallized from dichloromethane-heptane; wt. 0.127 g (30%), mp=155°-157°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04935515
Source datasetuspto-grants-1990_06
ORD IDord-019dcd9bad3c477e96013307c73dd38f
Source noteuspto-grants-1990_06