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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731373Generated: October 29, 2026

Sodium ethoxide → HCID 137194586, compound

https://huagongshe.com/reaction/731373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 57671240HCID 57671240—
SolventEthanolHCID 702—
ProductHCID 137194586HCID 1371945863.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of the crude 2-{[2-(7-methanesulfonylamino-1,1-dioxo-1,4-dihydro-1λ6-benzo[1,2,4]thiadiazin-3-yl)-acetyl]-methyl-amino}-cyclopentanecarboxylic acid ethyl ester in ethanol (20 mL) was treated with a 21% w/w solution of sodium ethoxide in ethanol (0.648 g) and stirred for 16 h at 60° C. Upon cooling, the reaction mixture was then quenched with 1.0 M aqueous hydrochloric acid solution (20 mL) and extracted with ethyl acetate (2×50 mL). The combined organic layers were washed with saturated aqueous sodium bicarbonate solution, dried over sodium sulfate, filtered, and dried in vacuo. The residue was purified by prep-HPLC [Column ODS-A 5μ 100 Å, 150×21.2 mm, 5 micron, 50%-100% in 13.5 min @ 22 mL/min flow rate, 0.05% trifluoroacetic acid in acetonitrile/0.05% trifluoroacetic acid in water] to afford the desired product, cis-N-[3-(4-hydroxy-1-methyl-2-oxo-2,4a,5,6,7,7a-hexahydro-1H-[1]pyrindin-3-yl)-1,1-dioxo-1,4-dihydro-1λ6-benzo[1,2,4]thiadiazin-7-yl]-methanesulfonamide (7.5 mg, 0.017 mmol, 3.4% over two steps), as a white solid. 1H NMR (400 MHz, DMSO-d6) δ: 1.49-1.69 (4H, m), 1.85-2.22 (3H, m), 2.88-3.20 (3H, m) 3.05 (3H, s), 3.90 (1H, bs), 7.50-7.64 (3H, m), 10.17 (1H, s). LC-MS (ESI) calcd for C17H20N4O6S2 440.08, found 441.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582626B2
Source datasetuspto-grants-2009_09
ORD IDord-aeba47be9d9f4d5282e24e74d48db9f2
Source noteuspto-grants-2009_09