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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252700Generated: November 2, 2026

N-(5-Iodo-4-methyl-2-thiazolyl)acetamide → HCID 86620380, compound

https://huagongshe.com/reaction/252700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(5-Iodo-4-methyl-2-thiazolyl)acetamideHCID 57417074—
Reactant5-Bromo-N-(2-hydroxyethyl)-3-pyridinesulfonamideHCID 61795523—
ProductHCID 86620380HCID 8662038023%

Reaction Steps

Using an analogous method to that described in Example 7, N-(5-iodo-4-methyl-1,3-thiazol-2-yl)acetamide was reacted with 5-bromo-N-(2-hydroxyethyl)pyridine-3-sulfonamide to give the title compound (Method A HPLC: retention time 4.0 minutes; 10 mg, 23%); 1H NMR Spectrum: (DMSOd6) 12.22 (1H, br s); 8.92 (1H, d); 8.86 (1H, d); 8.16 (1H, t); 7.96 (1H, br s); 4.73 (1H, t); 3.39 (2H, br q); 2.89 (2H, br t); 2.40 (3H, s); 2.17 (3H, s); Mass Spectrum: M+H+ 357.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868188B2
Source datasetuspto-grants-2011_01
ORD IDord-83ad2c1c82fb4ccd81e3b61fc120a503
Source noteuspto-grants-2011_01