HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713716Generated: October 30, 2026
Triethylamine hydrochloride → HCID 178452323, compound
https://huagongshe.com/reaction/713716
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Tert-butyl 4-(cyanomethyl)piperazine-1-carboxylate | HCID 21936030 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178452323 | HCID 178452323 | 63% |
Reaction Steps
To a stirred suspension of 1.50 g (6.66 mmol) of the title compound from Step A above in 25 mL of anhydrous toluene was added 1.38 g (10.0 mol) of triethylamine hydrochloride followed by 0.65 g (10 mmol) of sodium azide. The resulting mixture was heated to 80° C. for 12 h then cooled to ambient temperature. All volatiles were removed in vacuo, and the residue suspended in 5 mL of brine and 1.0 N aqueous hydrogen chloride solution was added until pH of ˜4 was achieved. The aqueous phase was extracted with chloroform and the combined organics were dried over magnesium sulfate and evaporated to dryness in vacuo. The residue was purified by silica gel chromatography eluting with a 0-100% acetone in hexanes gradient to afford the title compound (i-18) as white solid (1.1 g, 63%). 1H-NMR (500 MHz, DMSO-d) δ 3.82 (s, 2H), 3.29 (br s, 4H), 2.38-2.34 (m, 4H), 1.36 (s, 9H). LC-MS: m/z (ES) 269.0 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09186354B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-4bc4ae2f2bb9406ba7feab0f37ae1784 |
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| Source note | uspto-grants-2015_11 |
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