HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70337Generated: October 29, 2026
2-Aminoindane → HCID 58276358, compound
https://huagongshe.com/reaction/70337
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminoindane | HCID 76310 | — |
| Reactant | MeOH tetrahydrofuran | HCID 21899815 | — |
| Reactant | HCID 58276410 | HCID 58276410 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 58276358 | HCID 58276358 | — |
Reaction Steps
To a solution of [3-(3′-formyl-4-biphenylyl)-1H-1,2,4-triazol-1-yl]methyl 2,2-dimethylpropanoate (0.081 g, 0.22 mmol; I-X-17) and 2-aminoindane (0.045 mL, 0.35 mmol) in 1:1 THF/MeOH (2 mL) was added acetic acid (0.12 mL) and MP—BH3CN (ca. 0.67 mmol, Note 1). The mixture was stirred at room temperature overnight, resin was remove by filtration (THF wash) and the filtrate was concentrated in vacuo. The residue was partitioned between EtOAc/5% Na2CO3, layers were separated and the aqueous layer was extracted with EtOAc. Combined organics were washed (water, brine), dried over Na2SO4, and concentrated in vacuo. The residue was purified by flash chromatography (MeOH/CH2Cl2), affording the title compound. 1H NMR (400 MHz, CDCl3) δ ppm 1.20 (s, 9 H), 2.84 (dd, J=15.6, 6.4 Hz, 2 H), 3.20 (dd, J=15.6, 7.1 Hz, 2 H), 3.68-3.75 (m, 1 H), 3.93 (s, 2 H), 6.09 (s, 2 H), 7.08-7.23 (m, 4 H), 7.31-7.38 (m, 1 H), 7.41 (t, J=7.6 Hz, 1 H), 7.53 (d, J=7.6 Hz, 1 H), 7.63 (s, 1 H), 7.69 (d, J=8.3 Hz, 2 H), 8.19 (d, J=8.3 Hz, 2 H), 8.37 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822518B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-73dbbbf537394ce184ea6d8a98a5a143 |
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| Source note | uspto-grants-2014_09 |
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