HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037568Generated: October 31, 2026
Methanesulfonyl chloride → HCID 88415676, compound
https://huagongshe.com/reaction/1037568
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 67775937 | HCID 67775937 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 88415676 | HCID 88415676 | 77% |
Reaction Steps
To a solution of compound (viii) (9 mg, 0.02 mmol) in DCM (4 mL) at 0° C. were added DIPEA (30 μL, 0.17 mmol) and methanesulfonyl chloride (6 μL, 0.078 mmol). The reaction was stirred at 0° C. for 1 h, at which time it was diluted with DCM (12 mL) and saturated aqueous sodium bicarbonate (4 mL). The aqueous layer was separated and extracted with DCM (12 mL). The combined organic layers were washed with water (5 mL), dried (MgSO4) and evaporated to dryness. The residue was purified by flash column chromatography eluting with EtOAc/heptane (50-100%) to afford racemic 3-[5-cyclopropyl-3-(methylcarbamoyl)-2-(4-methylphenyl)-2H-indazol-6-yl]-3-(methylsulfonyl)propyl methanesulfonate (ix) as a white solid (8 mg, 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08546389B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-14a0951fb31f4b47add33ac819ad0a36 |
|---|
| Source note | uspto-grants-2013_10 |
|---|