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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252708Generated: October 31, 2026

Benzyloxyacetyl chloride → HCID 86620385, compound

https://huagongshe.com/reaction/252708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyloxyacetyl chlorideHCID 177085—
ReactantHCID 86620386HCID 86620386—
ProductHCID 86620385HCID 86620385—

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-benzyloxyacetyl chloride. The reaction product was purified by preparative HPLC (Method A) to give the title product (retention time 9.6 minutes); 1H NMR Spectrum: (DMSOd6+D2O) 8.56 (1H, d); 8.09 (1H, d); 8.03 (2H, br d); 7.83 (1H, t); 7.70 (2H, t); 7.31-7.26 (3H); 7.26-7.24 (2H); 4.41 (2H, AB system); 4.12 (1H, d); 3.86 (1H, d); 2.24 (3H, s); Mass Spectrum: M+H+ 529.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868188B2
Source datasetuspto-grants-2011_01
ORD IDord-25b3735ca41246568ef6f512e55650af
Source noteuspto-grants-2011_01