HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272875Generated: October 27, 2026
Hydrochloric Acid → 1-(5-(1H-1,2,4-Triazol-3-Yl)(1H-Indazol-3-Yl))-3-(2-Piperazinylethoxv)benzene
https://huagongshe.com/reaction/1272875
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | 3-(1-(Tetrahydro-2H-pyran-2-yl)-5-(1-trityl-1H-1,2,4-triazol-3-yl)-1H-indazol-3-yl)phenol | HCID 22479761 | — |
| Reactant | 2-(Tert-butyloxycarbonyl)piperazinylethanol | HCID 22480083 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(5-(1H-1,2,4-Triazol-3-Yl)(1H-Indazol-3-Yl))-3-(2-Piperazinylethoxv)benzene | HCID 20789036 | 52% |
Reaction Steps
Triphenylphosphine (0.694 g, 2.65 mmol), tetrahydrofuran (2.12 mL), 2-(tert-butyloxycarbonyl)piperazinylethanol (0.610 g, 2.65 mmol) and diethylazodicarboxylate (0.418 mL, 2.65 mmol) were added to 3-{1-perhydro-2H-pyran-2-yl-5-[1-(triphenylmethyl)(1,2,4-triazol-3-yl)]-1H-indazol-3-yl}phenol (0.400 g, 0.662 mmol). The mixture was stirred at ambient temperature for 23 h and poured into aqueous 6N hydrochloric acid (25 mL). After stirring at ambient temperature for 4 h, the mixture was extracted with ether (3×). The aqueous fraction was added to aqueous 6 N sodium hydroxide (25 mL) and the pH adjusted to 11. The solution was extracted with ethyl acetate (3×) and the organic fractions were combined and dried over anhydrous sodium sulfate, filtered and evaporated. The residue was purified by preparative HPLC (5–70% acetonitrile/water). The desired fractions were concentrated, dissolved in ethyl acetate, washed with aqueous sodium bicarbonate, dried over anhydrous sodium sulfate, filtered and evaporated to give the title compound (0.132 g, 52% yield) as the bis-trifluoroacetic acid salt. 1H NMR (D2O) δ 8.26 (s, 1H), 8.12 (s, 1H), 7.61 (d, 1H), 7.37 (d, 1H), 7.31 (m, 2H), 7.19 (m, 1H), 6.90 (m, 1H), 4.35 (m, 2H), 3.62 (m, 6H), 3.52 (m, 4H). ES-MS (m/z) 390 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07208513B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-c4fa81257522416fb8689ecc631f1010 |
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| Source note | uspto-grants-2007_04 |
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