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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055310Generated: October 29, 2026

Triethylamine → 5,5-Dioxo-2-(isopropylcarbonylamino)dibenzothiophene

https://huagongshe.com/reaction/2055310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyryl chlorideHCID 62325—
Reactant5,5-Dioxo-2-aminodibenzothiopheneHCID 14918529—
SolventDichloromethaneHCID 6344—
Product5,5-Dioxo-2-(isopropylcarbonylamino)dibenzothiopheneHCID 6931721646.1%

Reaction Steps

5,5-Dioxo-2-aminodibenzothiophene (J Med Chem, (1994), 37 (13), 2085-9; 231 mg, 1.0 mmol) was suspended in a solution of DCM (10 ml) and triethylamine (111 mg, 1.1 mmol). iso-Butyrylchloride (106.5 mg, 1.0 mmol) was added dropwise and the resultant mixture was stirred for 16 hours at ambient temperature. The mixture was evaporated in vacuo and the residue was purified by chromatography (Bond Elut column) eluting with 0-2.5% methanol in DCM to give the product as a colourless solid (139 mg). NMR: 10.38 (brs, 1H), 8.37 (s, 1H), 7.85-8.00 (m, 3H), 7.80 (d, 1H), 7.74 (d, 1H), 7.63 (t, 1H), 2.66 (m, 1H), 1.13 (d, 6H); m/z 302.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332492B2
Source datasetuspto-grants-2008_02
ORD IDord-819015c7fc6d4f9ab1a5524de2846ae6
Source noteuspto-grants-2008_02