Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660898Generated: October 31, 2026

Hydrochloric Acid → Methyl {4-[4-(tert.-butoxy)-4-oxo-n-butyl]-3-(4-chlorophenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl}-acetate

https://huagongshe.com/reaction/660898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactanttert-Butyl 4-bromobutanoateHCID 2757253—
ReactantMethyl[3-(4-chlorophenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-acetateHCID 136199105—
SolventDimethylformamideHCID 6228—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductMethyl {4-[4-(tert.-butoxy)-4-oxo-n-butyl]-3-(4-chlorophenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl}-acetateHCID 58011851—

Reaction Conditions

Temperature70 °C

Reaction Steps

Under an argon atmosphere, a solution of 130 mg (0.38 mmol) of the compound from Example 222A in 1 ml DMF and 2 ml DME at 0° C. is treated with 505 μl of an LiHMDS solution (1 M in THF, 505 μmol). The cooling bath is removed and the mixture stirred for 15 mins at RT before addition of 113 mg (505 μmol) of tert.-butyl 4-bromobutanoate. The mixture is stirred overnight at 70° C. After cooling, 0.5 ml of 1 N hydrochloric acid are added. The reaction mixture is then directly separated by preparative HPLC (Method 20). 48 mg (30% of theory) of the title compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084481B2
Source datasetuspto-grants-2011_12
ORD IDord-8360cfc82d2b4e2583cd03687fa090ef
Source noteuspto-grants-2011_12