HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757282Generated: November 2, 2026
HCID 10009261, compound → HCID 178428930, compound
https://huagongshe.com/reaction/1757282
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 10009261 | HCID 10009261 | — |
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178428930 | HCID 178428930 | — |
Reaction Steps
A mixture of 2-methyl-4-[(2'-(2-triphenylmethyl-2H-tetrazol-5-yl)biphenyl-4-yl)methoxy]quinoline (A) (890 mg) and a 7.5M solution of hydrogen chloride dioxane (10 ml) and water (1 ml) was allowed to stand for 72 hours. Volatile material was removed by evaporation and the residue was triturated with ether (2×50 ml). The ether was decanted off and the solid residue crystallised from isopropanol to give 2-methyl-4-[(2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methoxy]quinoline hydrochloride (370 mg), as a white solid, m.p. 188°-190° C.; NMR (d6 -DMSO): 2.92(s,3H), 5.63(s,2H), 7.21(d,2H), 7.56-7.87(m,8H), 8.07(dt,1H), 8.28(dd,1H), 8.32(dd,1H); mass spectrum [-ve FAB, DMSO/NBA]: 392 (M-H)-, 158; microanalysis found: C,66.0; H,4.6; N,15.5%; C24H19N5O.HCl.0.5H2O requires: C,65.7; H,4.8; N,16.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05444071 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-5a5677f2991e415a8047215b40e5dc8a |
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| Source note | uspto-grants-1995_08 |
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