HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 603971Generated: October 30, 2026
Dichloromethane → HCID 21962365, compound
https://huagongshe.com/reaction/603971
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2-Chlorophenyl)methanesulfonyl chloride | HCID 2757801 | — |
| Reactant | HCID 21962279 | HCID 21962279 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21962365 | HCID 21962365 | — |
Reaction Steps
[(2-chlorophenyl)methyl]sulfonyl chloride (0.14 g, 0.6 mmol) was added to a mixture of ethyl 4-{2-[2-(2-Aminoethyl)-1-benzhydryl-5-chloro-1H-indol-3-yl]-ethoxy}-2-fluoro-benzoate (Step 6, Example 190, 0.12 g, 0.2 mmol) and K2CO3 (0.11 g, 0.8 mmol) in CH2Cl2 (2 mL) and water (1 mL) with stirring. After 2 hour at room temperature, the mixture was extracted with CH2Cl2 (10 mL) and the extract was washed with 0.5 N NaOH, and brine and dried over sodium sulfate. The CH2Cl2 solution was filtered through silica gel and the filtrate was evaporated. The resulting residue was triturated with a mixture of ether and hexanes to give 0.07 g of ethyl 4-{2-[1-benzhydryl-5-chloro-2-(2-{[(2-chlorobenzyl)sulfonyl]amino}ethyl)-1H-indol-3-yl]ethoxy}-2-fluorobenzoate as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07906548B2 |
|---|
| Source dataset | uspto-grants-2011_03 |
|---|
| ORD ID | ord-6982a4c101a54565b07d49d82dacc9b6 |
|---|
| Source note | uspto-grants-2011_03 |
|---|