HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710031Generated: October 26, 2026
Chlorosuccinimide → HCID 86706743, compound
https://huagongshe.com/reaction/710031
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(Prop-2-ynyloxy)pyridine | HCID 11423622 | — |
| Reactant | HCID 86706742 | HCID 86706742 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 86706743 | HCID 86706743 | 55.2% |
Reaction Steps
To a DMF (60 mL) solution of the compound (8.57 g) obtained in Example 2-(1), NCS (5.341 g) was added in small portions at 0° C. and the mixture was stirred at room temperature for an hour. The reaction mixture was cooled to 0° C. and after adding a solution of 3-(prop-2-yn-1-yloxy)pyridine (2.663 g) in THF (5 mL) and a solution of Et3N (5.6 mL) in THF (15 mL), the resulting mixture was stirred at room temperature for 14 hours. The reaction mixture was added to saturated aqueous sodium bicarbonate (200 mL), followed by extraction with AcOEt (200 mL). The resulting organic layer was washed with brine (200 mL), dried (MgSO4), filtered and concentrated to give a crude product, which was further purified by neutral silica gel chromatography (AcOEt/hexane) to give the titled compound (3.81 g, pale yellow solid.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181229B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-eb8e1c3588984a42b6af5122cccf4046 |
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| Source note | uspto-grants-2015_11 |
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