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Sodium Hydroxide → sodium 2-{7-[(aminosulfonyl)amino]-1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl}-7-fluoro-3-oxo-4,4-dipropyl-3,4-dihydronaphthalen-1-olate

HRID 494485
Notes
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Reaction equation

HRID 494485 reaction equation
[F:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([CH2:34][CH2:35][CH3:36])([CH2:31][CH2:32][CH3:33])[C:7](=[O:30])[C:8]([C:13]3[NH:18][C:17]4[CH:19]=[CH:20][C:21]([NH:23][S:24]([NH2:27])(=[O:26])=[O:25])=[CH:22][C:16]=4[S:15](=[O:29])(=[O:28])[N:14]=3)=[C:9]2[OH:12])=[CH:4][CH:3]=1.[OH-].[Na+:38]>C(#N)C>[NH2:27][S:24]([NH:23][C:21]1[CH:20]=[CH:19][C:17]2[NH:18][C:13]([C:8]3[C:7](=[O:30])[C:6]([CH2:31][CH2:32][CH3:33])([CH2:34][CH2:35][CH3:36])[C:5]4[C:10](=[CH:11][C:2]([F:1])=[CH:3][CH:4]=4)[C:9]=3[O-:12])=[N:14][S:15](=[O:29])(=[O:28])[C:16]=2[CH:22]=1)(=[O:25])=[O:26].[Na+:38]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 136337523N-[3-(7-fluoro-1-hydroxy-3-oxo-4,4-dipropyl-3,4-dihydronaphthalen-2-yl)-1,1-dioxido-4H-1,2,4-benzothiadiazin-7-yl]sulfamide

Product 1

HCID 68874514sodium 2-{7-[(aminosulfonyl)amino]-1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl}-7-fluoro-3-oxo-4,4-dipropyl-3,4-dihydronaphthalen-1-olateYield 94.6%

Reagents, catalysts & solvents 1

HCID 6342
Acetonitrile
Solvent

Procedure

A solution of Example 17E (13 mg) was dissolved in acetonitrile (1 mL) and treated with sodium hydroxide solution (1.0 N, 24.3 μL, 0.0243 mmol). After stirring for 30 min, the solution was frozen and lyophilized to afford the title compound as a fluffy grey solid (12.8 mg, 55% overall). 1H NMR (300 MHz, DMSO-d6): δ 0.65 (m, 8 H) 0.86 (d, J=2.94 Hz, 2 H) 1.65 (d, J=3.68 Hz, 2 H) 2.05 (m, 2 H) 7.43 (m, 6 H) 9.58 (s, 1 H) 15.21 (s, 1 H).

Workup

  1. temperaturethe solution was frozen

Sources & evidence

ORD record
ord-d2b2079566584a5fae438dfe9aff5bb8
Source dataset
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07538105B2

Reaction notes

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