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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224940Generated: October 30, 2026

Sodium Hydroxide → Sodium (4r)-2-[7-({[6-(acetylamino)-2-naphthyl]sulfonyl}amino)-1,1-dioxido-4h-1,2,4-benzothiadiazin-3-yl]-4-methyl-4-(3-methylbutyl)-3-oxo-3,4-dihydronaphthalen-1-olate

https://huagongshe.com/reaction/2224940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantn-{6-[({3-[(4r)-1-Hydroxy-4-methyl-4-(3-methylbutyl)-3-oxo-3,4-dihydronaphthalen-2-yl]-1,1-dioxido-4h-1,2,4-benzothiadiazin-7-yl}amino)sulfonyl]-2-naphthyl}acetamideHCID 136384631—
SolventWaterHCID 962—
ProductSodium (4r)-2-[7-({[6-(acetylamino)-2-naphthyl]sulfonyl}amino)-1,1-dioxido-4h-1,2,4-benzothiadiazin-3-yl]-4-methyl-4-(3-methylbutyl)-3-oxo-3,4-dihydronaphthalen-1-olateHCID 13172690099.9%

Reaction Steps

A mixture of Example 104A (5.0 mg, 0.0072 mmol) and 0.998 M sodium hydroxide (0.0072 mL, 0.0072 mmol) in water (1 mL) was stirred at rt for 16 h. The reaction mixture was concentrated in vacuo to give the title compound (5.1 mg, quant. yield). 1H NMR (300 MHz, DMSO-d6) δ 0.42 m, 1 H) 0.66 (t, J=6.80 Hz, 6 H) 0.75 m, 1 H) 1.26 (m, 1 H) 1.36 (s, 3 H) 1.73 m, 1 H) 2.10 m, 4 H) 7.21 (d, J=9.93 Hz, 1 H) 7.31 (m, J=8.46, 2.21 Hz, 2 H) 7.38 (d, J=2.21 Hz, 1 H) 7.46 m, 2 H) 7.67 m, 2 H) 8.01 m, 3 H) 8.30 (s, 1 H) 8.37 (s, 1 H) 10.31 (s, 1 H) 10.51 (s, 1 H) 15.31 (s, 1 H). MS (ESI+) m/z 709.1 (M+H)+, 687.6 (M+H—Na)+, 704.1 (M−Na+ NH4)+, (ESI−) m/z 707.1 (M−H)−, 685.0 (M−H—Na)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378414B2
Source datasetuspto-grants-2008_05
ORD IDord-2daae7c806fc490cbed5b62c0d855c2b
Source noteuspto-grants-2008_05