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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181156Generated: November 3, 2026

Benzylamine → HCID 13007231, compound

https://huagongshe.com/reaction/1181156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantDiisopropyl EtherHCID 7914—
ReactantHCID 69424420HCID 69424420—
SolventEthanolHCID 702—
ProductHCID 13007231HCID 1300723142%

Reaction Steps

A mixture of 1-(3,5-dibromo-4-nitropyrazol-1-yl)-propane-1,2-diol (3-4) (31 g, 898 mmol), EtOH (420 ml) and benzylamine (138 g, 1.26 mol) was refluxed for 1.5 hours. The reaction medium was concentrated to the maximum under reduced pressure. 100 ml of DCM were added to the residue. The organic phase was washed with dilute acid (5×50 ml). The organic phase was dried over Na2SO4 and the solvent was evaporated off under reduced pressure. The brown oil obtained was treated with diisopropyl ether at 0° C. to give the 3-(5-benzylamino-3-bromo-4-nitropyrazol-1-yl)propane-1,2-diol (14.1 g, 42%) in the form of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285136B2
Source datasetuspto-grants-2007_10
ORD IDord-535201fe3cc143289faa4a4d75cb0b39
Source noteuspto-grants-2007_10