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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476510Generated: October 30, 2026

HCID 15079650, compound → HCID 15079652, compound

https://huagongshe.com/reaction/476510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15079650HCID 15079650—
ReactantSodium NitriteHCID 23668193—
CatalystCopper SulfateHCID 24462—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
SolventHCID 21552640HCID 21552640—
ProductHCID 15079652HCID 1507965228.2%

Reaction Steps

While maintaining a temperature of 5° C. to 10° C., 1.03 g (0.015 mole) of sodiuM nitrite dissolved in 10 ml of water was added to a stirred mixture of 4.76 g (0.0125 mole) of 1-[5-(4-aminophenoxy)-4-chloro-2-fluorophenyl]-1,4-dihydro-4-(3-fluoropropyl)-5H-tetrazol-5-one (prepared by the method of Steps A and B of Example 1 in 6 ml of concentrated sulfuric acid. The resultant mixture was stirred at 6° C. for 30 minutes. This mixture was added to a refluxing mixture of 37.5 g (0.150-mole) of copper II sulfate in 70 ml of xylene/toluene (50/50) and 100 ml of water. After complete addition, the mixture was stirred and heated at reflux for one hour. The mixture was cooled to room temperature and the phases were allowed to separate. The organic phase was extracted with an aqueous sodium hydroxide solution (6.0 g of sodium hydroxide in 250 ml of water). The basic extract was acidified with concentrated hydrochloric acid forming a precipitate. This mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure to yield 1.35 g of 1-[4-chloro-2-fluoro-5-(4-hydroxyphenoxy)phenyl]-1,4-dihydro-4-(3-fluoropropyl)-5H-tetrazol-5-one as a solid, m.p. 157°-159° C., compound 3 of Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04885025
Source datasetuspto-grants-1989_12
ORD IDord-61fb1e8c04404d3db2cef5a721edebb5
Source noteuspto-grants-1989_12