Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602562Generated: November 1, 2026

Thionyl Chloride → (5-Tert-butyl-2-methoxy-phenyl)-[5-(2,6-diethyl-phenyl)-pyrrolo-[2,3-c]pyridine-1-yl]-methanone

https://huagongshe.com/reaction/602562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Tert-Butyl-2-Methoxybenzoic AcidHCID 7010315—
Reactant5-(2,6-diethyl-phenyl)-1H-pyrrolo[2,3-c]pyridineHCID 11673246—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product(5-Tert-butyl-2-methoxy-phenyl)-[5-(2,6-diethyl-phenyl)-pyrrolo-[2,3-c]pyridine-1-yl]-methanoneHCID 5826995868.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

Thionyl chloride (0.3 mL, excess) is added dropwise to a solution of 5-tert-butyl-2-methoxy-benzoic acid (30 mg, 0.2 mmol) in CH2Cl2 (1 mL) at room temperature. The mixture is heated to 60° C. for 1.5 hours. The solvent is removed to dryness. A solution of 5-(2,6-diethyl-phenyl)-1H-pyrrolo[2,3-c]pyridine (10 mg, 0.04 mmol) and N,N-diisopropylethylamine (0.2 mL, excess) in THF (1 mL) is added to the residue. The mixture is stirred at room temperature for 16 hours. The solvent is removed to dryness in vacuo. The crude product is purified by PTLC and eluted with 20% EtOAc in hexane to give 12 mg of (5-tert-butyl-2-methoxy-phenyl)-[5-(2,6-diethyl-phenyl)-pyrrolo-[2,3-c]pyridine-1-yl]-methanone. 1H NMR (CDCl3) 7.56-6.98 (m, 9H), 6.60-6.58 (d, 1H), 3.81 (s, 3H), 2.41-2.24 (q, 4H), 1.31 (s, 9H), 1.08-1.00 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906528B2
Source datasetuspto-grants-2011_03
ORD IDord-777955bd3f224eeab416135fa2fd8703
Source noteuspto-grants-2011_03