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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719557Generated: October 30, 2026

HCID 178441767, compound → HCID 178441772, compound

https://huagongshe.com/reaction/719557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178441767HCID 178441767—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 178441772HCID 17844177281%

Reaction Steps

A 92 mg sample of 5-[4′-[[5-butyl-3-(dimethoxymethyl)-1H-1,2,4-triazol-1-yl]methyl][1,1′-biphenyl]-2-yl]-1H-tetrazole from Example 24 was dissolved in 20 ml of ethanol and 2 ml of 3N HCl. The reaction was stirred at ambient temperature for 3 days. The solvent was removed in vacuo. Lyophilization from acetonitrile/water gave 70 mg (81%) of 5-butyl-1-[2′-(1H-tetrazol-5-yl)[1,1′-biphenyl]-4-ylmethyl]-1H-1,2,4-triazole-3-carboxaldehyde as the colorless hydrochloride salt: NMR (CDCl3) δ 0.89 (t, J=8 Hz, 3H), 1.30–1.44 (m, 2H), 1.66–1.78 (m, 2H), 2.78 (t, J=8 Hz, 2H), 5.38 (s, 2H), 7.17 (q, J=8 Hz, 4H), 7.40 (d, J=8 Hz, 1H), 7.50–7.64 (m, 2H), 8.02 (d, J=8 Hz, 1H); MS (FAB) m/e (rel intensity) 388 (36), 235 (42), 207 (100), 192 (50); HRMS. Calc'd for M+Li: 395.2046. Found: 395.2049.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132437B2
Source datasetuspto-grants-2006_11
ORD IDord-25be403787b54dccb9260bc109a8805c
Source noteuspto-grants-2006_11