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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583298Generated: November 4, 2026

Potassium Bromide → 4-[1-(Hexyloxycarbonyloxy)ethoxy]-2-methyl-N-(2-pyridyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-Dioxide

https://huagongshe.com/reaction/1583298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BromideHCID 253877—
Reactant1-Chloroethyl Hexyl CarbonateHCID 13506637—
ReactantIsopropanol hexaneHCID 21585144—
ReactantPiroxicamHCID 54676228—
Product4-[1-(Hexyloxycarbonyloxy)ethoxy]-2-methyl-N-(2-pyridyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-DioxideHCID 13506667—

Reaction Steps

By the procedure of Example 11, piroxicam (3.00 g, 9.1 mmol) and alpha-chloroethyl hexyl carbonate (2.85 g, 13.6 mmol) were converted to chromatographed title product, isolated as a yellow solid which was crystallized from isopropyl alcohol/hexane (280 mg, 0.5 mmol, 6.1%): mp 86°-87° C.; IR (KBr) 1764, 1678 cm-1 ; 1H NMR (CCl3) delta 0.87 (t, J=7 Hz, 3H), 1.05-1.39 (m, 6H), 1.41-1.60 (m, 2H), 1.75 (d, J=6 Hz, 3H), 3.10 (s, 3H), 4.00 (t, J=7 Hz, 2H), 6.36 (q, J=6 Hz, 1H), 7.06-7.17 (m, 1H), 7.63-7.86 (m, 5H), 8.31-8.42 (m, 2H), 9.39 (br s, 1H); precise mass calcd for C24H29N3O7S m/e 503.1737, found 503.1761.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04551452
Source datasetuspto-grants-1985_11
ORD IDord-94f620f29ff141b5b1b61451c538b220
Source noteuspto-grants-1985_11