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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479056Generated: November 3, 2026

Methanesulfonyl chloride → HCID 71610198, compound

https://huagongshe.com/reaction/1479056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 71610126HCID 71610126—
SolventDichloromethaneHCID 6344—
ProductHCID 71610198HCID 7161019836.2%

Reaction Steps

To a solution of Example 3 (100 mg; 0.23 mmol; 1 eq.) and TEA (82 μL; 0.59 mmol; 2.5 eq.) in DCM (3 mL) at 0° C. was added methanesulfonyl chloride (22 μL; 0.28 mmol; 1.2 eq.). The reaction mixture was stirred at room temperature for 16 hours. The solution was diluted with DCM, washed successively with 0.1M HCl and brine, dried over magnesium sulfate and concentrated in vacuo. Purification by mass directed preparative HPLC afforded the title compound (42 mg, 35%) as a white solid. 1H NMR (CDCl3) δ 7.43-7.34 (m, 2H), 7.12-7.05 (m, 1H), 7.01-6.96 (m, 1H), 4.98 (s, 0.7H), 4.97 (s, 1.3H), 4.69-4.64 (m, 3H), 3.39-3.32 (m, 2H), 3.18-3.08 (m, 2H), 2.91 (s, 2H), 2.86 (s, 1H), 2.72 (s, 3H), 2.70 (s, 1H), 2.62 (s, 2H), 2.00-1.93 (m, 4H). HPLC (max plot) 98.0%, Rt 3.61 min. UPLC/MS: (MS+) 504.4 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403835B2
Source datasetuspto-grants-2016_08
ORD IDord-3688142a4ce345629737f3c35f9d1056
Source noteuspto-grants-2016_08