HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanesulfonylchloride, 2-chloro- → HCID 69842640, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanesulfonylchloride, 2-chloro- | HCID 15385 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178504922 | HCID 178504922 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69842640 | HCID 69842640 | 116.5% |
Reaction Steps
2-Chloroethanesulfonyl chloride (1.85 g, 11.4 mmol) was added to a solution of Compound C of Example 248 (1.0 g, 3.79 mmol) and DIEA (2.6 mL, 15.16 mmol) in dichloromethane (16 mL) at 0° C. under argon. After stirring for 16 hr, the reaction was diluted with chloroform (20 mL) and NaHCO3 (5 mL). The layers were separated, the aqueous layer was extracted with chloroform (2×50 mL). The combined organic extracts were washed with NaHCO3 (2×20 mL) and brine (2×50 mL), dried over MgSO4, filtered and concentrated, to afford Compound A (1.55 g, 116.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06455523B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-e474d27757da45809695accda966ef56 |
| Source note | uspto-grants-2002_09 |