HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuryl chloride → HCID 57812309, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Isocyanate | HCID 105034 | — |
| Reactant | Carbonochloridate | HCID 21226386 | — |
| Reactant | HCID 67401992 | HCID 67401992 | — |
| Catalyst | Isocyanate | HCID 105034 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57812309 | HCID 57812309 | — |
Reaction Steps
General procedure Q for N-alkylation/acylation, using isocyanate, chloroformate, and sulfonyl chloride species: To a solution of 7-[(1R)-1-(2,6-dichloro-3-fluorophenyl)ethoxy]-3-[1-(piperidin-4-yl)-1H-pyrazol-4-yl]furo[3,2-c]pyridin-6-amine dihydrochloride (10.6 mg, 0.0188 mmol, 1 eq) and DIPEA (26 μL, 0.15 mmol, 8 eq) in DMF (1 mL), one drop of the isocyanate, chloroformate, or sulfonyl chloride (approx. 0.0346 mmol, 1.8 eq) was added and the reaction was stirred at rt for 1 h. The DMF solution was syringe filtered and submitted directly to the analytical department for purification by MDPS. Fractions containing product were pooled together and all solvent was removed using the SpeedVac to give the title material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022206B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-800a723f154943c6bc0be9168f22aa91 |
| Source note | uspto-grants-2011_09 |