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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416212Generated: November 2, 2026

Dichloromethane → HCID 10217697, compound

https://huagongshe.com/reaction/2416212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPiperidineHCID 8082—
ReactantPivaloyl chlorideHCID 62493—
ReactantHCID 22638593HCID 22638593—
SolventWaterHCID 962—
ProductHCID 10217697HCID 10217697—

Reaction Steps

To a suspension of 3-(2-benzenesulfonylmethyl-thiazol-4-yl)-1H-quinolin-2-one-7-carboxylic acid (Example 8733 step (h), 0.1 g, 0.2 mmol) and 5 mL of anhydrous CH2Cl2 was added TEA (0.2 mL, 1.4 mmol) and pivaloyl chloride (0.1 mL, 0.8 mmol). The solution was stirred overnight at RT. The reaction was now homogenous and piperidine (0.5 mL, 5.1 mmol) was added. After 6 h, the reaction was diluted with H2O. The aqueous solution was extracted with EtOAc (6×). The combined EtOAc layers were washed with brine, dried over MgSO4, and concentrated in vacuo. The solid was suspended in a minimum of EtOAc and filtered to give a solid. MS m/z: 494.1 (M+1). Anal. Calc'd for C25H23N3O4S2.0.5H2O: C, 59.74; H, 4.81; N, 8.36. Found: C, 59.64; H, 4.82; N, 8.30.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06822097B1
Source datasetuspto-grants-2004_11
ORD IDord-04803e4d088f46e2af59bccb5f8c8066
Source noteuspto-grants-2004_11