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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164744Generated: October 30, 2026

5-Bromo-1-methyl-1H-tetrazole → HCID 20403203, compound

https://huagongshe.com/reaction/2164744

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-1-methyl-1H-tetrazoleHCID 12797446—
Reactant1-Amino-4-{3-[(piperidin-1-yl)methyl]phenoxy}butan-2-olHCID 20246015—
SolventEthanolHCID 702—
ProductHCID 20403203HCID 2040320355.6%

Reaction Steps

A solution of 1-amino-4-[3-(1-piperidinylmethyl)phenoxy]-2-butanol (1.39 g) and 5-bromo-1-methyl-1H-tetrazole (0.82 g) in absolute ethanol (10 ml) was heated in an autoclave at 125° for 18 h. The solution was evaporated and the residue dissolved in 1M hydrochloric acid (25 ml). The acidic solution was washed with ethyl acetate, basified with excess sodium carbonate and extracted with ethyl acetate. The extract was dried and evaporated to leave a solid which was triturated with dry diethyl ether to give a white solid (1.0 g). This solid was recrystallised from methyl acetate-light petroleum (b.p. 60°-80°) to give the title compound (0.6 g) as white crystals, m.p. 138°-9°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04507296
Source datasetuspto-grants-1985_03
ORD IDord-68a4605673704cfebaac9762fb2aff03
Source noteuspto-grants-1985_03