HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573697Generated: October 30, 2026
(4-Chlorophenyl)methanesulfonyl chloride → HCID 68323916, compound
https://huagongshe.com/reaction/573697
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (4-Chlorophenyl)methanesulfonyl chloride | HCID 227304 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 68323863 | HCID 68323863 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68323916 | HCID 68323916 | 13.2% |
Reaction Steps
To a stirred solution of 2,6-dimethyl-3-[3-(methyloxy)phenyl]thieno[2,3-b]pyridin-4-amine (100 mg, 0.352 mmol) (Description 4) in THF (2 mL) cooled in an ice bath was added LiHMDS (1M solution in THF) (0.774 mL, 0.774 mmol). The reaction mixture was stirred at RT for 45 min before the addition of 4-chlorobenzylsulfonyl chloride (198 mg, 0.879 mmol). The reaction mixture was then stirred at RT for a further 16 h and was then cooled in an ice bath before the addition of LiHMDS (1M solution in THF) (0.352 mL, 0.352 mmol). The reaction mixture was stirred at RT for 1 h before the addition of 4-chlorobenzylsulfonyl chloride (79.2 mg, 0.352 mmol). The reaction mixture was stirred at RT for a further 16 h and then diluted with water (10 mL) and the aqueous layer extracted with DCM (3×20 mL). The combined organic extracts were dried over a phase separating column and concentrated. The residue was purified by MDAP (basic conditions), to afford the title compound (22 mg). LCMS (A) m/z: 473 [M+1]+, Rt 1.42 min (basic).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09029545B2 |
|---|
| Source dataset | uspto-grants-2015_05 |
|---|
| ORD ID | ord-55a5462831054be58e18d367d90ded9c |
|---|
| Source note | uspto-grants-2015_05 |
|---|