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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755927Generated: November 2, 2026

HCID 178429713, compound → HCID 178429714, compound

https://huagongshe.com/reaction/1755927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178429713HCID 178429713—
SolventWaterHCID 962—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 178429714HCID 17842971494.9%

Reaction Steps

N-[(7-Mercapto-5-methyl-s-triazolo[1,5-a]-pyrimidin-2-yl)methyl]-2,2-diphenyl-1,3-benzodioxol-5-carboxamide (22.7 g) are stirred for 1 hour in 210 ml of trifluoroacetic acid and 5 ml of water. A small amount of insoluble material is filtered off and the mother liquor is evaporated to dryness. The yellow residue is treated with 900 ml of ethyl acetate, stirred in an ultrasound bath for 1 hour and subsequently cooled in an ice bath. The yellow solid is filtered off and dried in a vacuum at 40° C. There are obtained 14.4 g of 3,4-dihydroxy-N-(7-mercapto-5-methyl[1.2.4]triazolo[1,5-a]pyrimidin-2-ylmethyl)-benzamide as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05438052
Source datasetuspto-grants-1995_08
ORD IDord-569a1141dc724b7fae7bad53dbca3ada
Source noteuspto-grants-1995_08