Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421855Generated: November 2, 2026

Ammonium Acetate → HCID 57617810, compound

https://huagongshe.com/reaction/2421855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantHCID 67242918HCID 67242918—
SolventDimethylformamideHCID 6228—
ProductHCID 57617810HCID 576178106%

Reaction Steps

N-(2-hydroxyphenyl)-4-(4-(trifluoromethyl)phenylsulfonyl)-3,4-dihydro-2H-benzo[b][1,4]thiazine-6-carboxamide (25 mg, 51 μmol) was dissolved in 1 mL of DMF. Ammonium acetate (39 mg, 506 μmol) was added and the reaction was subjected to microwave irradiation (150° C., 25 min). LCMS analysis of the reaction mixture showed consumption of starting material. The reaction mixture was diluted with saturated aqueous sodium bicarbonate (1 mL) and EtOAc (2 mL). The organic layer was removed and the aqueous layer extracted with EtOAc (2 mL). The organic layers were combined, dried over anhydrous Na2SO4, filtered and evaporated. The residue was purified by flash column chromatography with gradient elution of hexanes with 10-60% EtOAc to provide 2-(4-(4-(trifluoromethyl)phenylsulfonyl)-3,4-dihydro-2H-benzo[b][1,4]thiazin-6-yl)benzo[d]oxazole (1.4 mg, 2.9 μmol, 6% yield) as a yellow oil. LCMS (+ESI) m/z=477.4 [M+H]+; 1H-NMR (CDCl3) δ 7.7-7.9 (m, 6H), 7.40 (d, 2H), 7.30 (d, 1H), 7.05 (dd, 1H), 6.80 (d, 1H), 3.50 (t, 2H), 3.05 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960376B2
Source datasetuspto-grants-2011_06
ORD IDord-6689566ba1b64687a0bc9a1b2cd1ab36
Source noteuspto-grants-2011_06