HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 5-Chloro-6-((2-oxo-1-oxa-3-azaspiro[4.5]decan-8-yl)methoxy)pyridine-3-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5,6-Dichloropyridine-3-sulfonamide | HCID 4730921 | — |
| Reactant | 8-(Hydroxymethyl)-1-oxa-3-azaspiro[4.5]decan-2-one | HCID 57576531 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Chloro-6-((2-oxo-1-oxa-3-azaspiro[4.5]decan-8-yl)methoxy)pyridine-3-sulfonamide | HCID 67126698 | — |
Reaction Steps
To a solution of EXAMPLE 385C (325 mg, 1.755 mmol) in a mixture of tetrahydrofuran (16 mL) and N,N-dimethylformamide (8 mL) was added sodium hydride (281 mg, 7.02 mmol) and the mixture was stirred for 30 minutes. 5,6-Dichloropyridine-3-sulfonamide (389 mg) was added and the reaction was stirred for 42 hours. The reaction was quenched with water (5 mL) and concentrated. The residue was diluted with 75% brine (200 mL) and extracted with methylene chloride (3×200 mL). The organics were dried over sodium sulfate, filtered, and concentrated. The residue was purified on silica gel and eluted with a 1, 5, and 10% methanol in methylene chloride step gradient to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09034875B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-af37d3b9bacf41fb93960001a1ffa98c |
| Source note | uspto-grants-2015_05 |