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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774647Generated: November 1, 2026

Acetyl chloride → (2-Bromo-4-fluoro-6-{6-oxo-8-thia-4,5-diazatricyclo[7.4.0.02,7]trideca-1 (9),2 (7),3-trien-5-yl}phenyl)methyl acetate

https://huagongshe.com/reaction/1774647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant(4-Fluoro-2-{6-oxo-8-thia-4,5-diazatricyclo[7.4.0.02,7]trideca-1(9),2(7),3-triene-5-yl}-6-(bromo)phenyl)carbinolHCID 118116415—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(2-Bromo-4-fluoro-6-{6-oxo-8-thia-4,5-diazatricyclo[7.4.0.02,7]trideca-1 (9),2 (7),3-trien-5-yl}phenyl)methyl acetateHCID 58044224—
Product6,7,8,9-Tetrahydrobenzo[4,5]thieno[2,3-d]pyridazin-4(3H)-oneHCID 67016553—

Reaction Steps

8-thia-4,5-diazatricyclo[7.4.0.02,7]trideca-1(9),2(7),3-trien-6-one was prepared following the procedures of U.S. Pat. No. 8,716,274, Example 191d and converted to (4-fluoro-2-{6-oxo-8-thia-4,5-diazatricyclo[7.4.0.02,7]trideca-1(9),2(7),3-triene-5-yl}-6-(bromo)phenyl)carbinol 108a. To a mixture of 108a (4.1 g, 10 mmol) and Et3N (1.95 mL, 14 mmol) in THF (50 mL) was added AcCl (0.85 mL, 12 mmol). The mixture was stirred at rt for 1 h, diluted with water and extracted with EA. The combined organic layers were dried over Na2SO4, filtered and concentrated to give compound 108b (4.0 g) as yellow solid. MS-ESI: [M+H]+ 451.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260415B2
Source datasetuspto-grants-2016_02
ORD IDord-8a665bad32ad42eda8a5e21260cb1e6f
Source noteuspto-grants-2016_02