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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457928Generated: November 2, 2026

Benzyl Bromide → HCID 22101205, compound

https://huagongshe.com/reaction/1457928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 15703582HCID 15703582—
SolventDimethylformamideHCID 6228—
ProductHCID 22101205HCID 22101205—

Reaction Steps

To a solution of 3-amino-1benzyl-4-ethoxycarbonylpyrazole (0.5 g) in DMF (10 ml), was added 60% NaH (0.082 g). After stirring for 5 min at room temperature, benzyl bromide (0.307 ml) was added, and the mixture was stirred for 1 h at room temperature. The reaction mixture was evaporated under reduced pressure followed by silica-gel column chromatography (toluene/ ethyl acetate=50/1) to give 3-benzylamino-1-benzyl-4-ethoxycarbonylpyrazole (0.3 g). This intermediate was derived to the title compound by the similar method to Reference Example 1 (yield 31%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849779
Source datasetuspto-grants-1998_12
ORD IDord-34177f4873c046c29d199d60c6a594fb
Source noteuspto-grants-1998_12