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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480327Generated: October 29, 2026

Triethylamine → HCID 57291699, compound

https://huagongshe.com/reaction/480327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 57003689HCID 57003689—
SolventDichloromethaneHCID 6344—
ProductHCID 57291699HCID 57291699115.5%

Reaction Steps

To a solution of 3-(3-{[3-(3-chloro-phenyl)-propyl]- amino}-propyl)-benzoic acid methyl ester (50.3 mg, 0.145 mmol) and triethylamine (32.4 mg, 0.32 mmol) in CH2Cl2 (10 mL) was added methanesulfonyl chloride (18.3 mg, 0.16 mmol) at 0° C. The reaction mixture was stirred for 24 h at room temperature and was diluted with CH2Cl2. The organic solution was washed consecutively with aqueous HCl (5.5%, 1×), H2O (1×), NaHCO3 (1×) and brine (1×). The organic solution was dried over MgSO4, filtered, and concentrated to afford the title product of Step A as an oil (71 mg). MS 424 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06649657B2
Source datasetuspto-grants-2003_11
ORD IDord-c27aa1738853494586824ef836b2d81f
Source noteuspto-grants-2003_11