HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876412Generated: October 30, 2026
Trimethylsilyl isocyanate → HCID 58303674, compound
https://huagongshe.com/reaction/876412
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyl isocyanate | HCID 70696 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 58303695 | HCID 58303695 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58303674 | HCID 58303674 | 64% |
Reaction Steps
To a solution of 2-([1,2,4]triazolo[4,3-a]pyridin-3-yl)-8-(piperidin-4-yloxy)quinoline (prepared as described in Example 9, 46 mg, 0.133 mmol) in CH2Cl2 (5 mL) were added DIEA (116 μL, 0.67 mmol), DMAP (2 mg, 0.01 mmol), and TMS-isocyanate (104 μL, 0.67 mmol). The reaction mixture was stirred at ambient temperature for 16 hours then partitioned between saturated NaHCO3 and CH2Cl2. The aqueous layer was extracted with CH2Cl2 and the combined organic phases were washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified by flash column chromatography with gradient elution (CH2Cl2 to 1% MeOH/CH2Cl2 to 3% MeOH/CH2Cl2) to afford desired product (33 mg, 64%) as a colorless glass. MS ESI (+) m/z 411.2 (M+Na+) detected.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08987251B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-b66a84bac29145198ff5f581f1be4dd1 |
|---|
| Source note | uspto-grants-2015_03 |
|---|