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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252711Generated: November 1, 2026

Methoxyacetyl chloride → HCID 86620389, compound

https://huagongshe.com/reaction/252711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxyacetyl chlorideHCID 96623—
ReactantHCID 86620386HCID 86620386—
ProductHCID 86620389HCID 86620389—

Reaction Steps

Using an analogous method to that described in Example 51, N-[5-(2-amino-4-methyl-1,3-thiazol-5-yl)-2-chloropyridin-3-yl]benzenesulfonamide was reacted with 2-methoxyacetyl chloride. The reaction product was purified by preparative HPLC (Method A) to give the title product (retention time 7.0 minutes); 1H NMR Spectrum: (DMSOd6+D2O) 8.59 (1H, d); 8.14 (1H, d); 8.03 (2H, d); 7.83 (1H, t); 7.70 (2H, t); 4.01 (1H, d); 3.72 (1H, d); 3.18 (3H, s); 2.27 (3H, s); Mass Spectrum: M+H+ 453.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868188B2
Source datasetuspto-grants-2011_01
ORD IDord-8c2e0c0334394105aa0742beb4cd1aa9
Source noteuspto-grants-2011_01