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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060363Generated: October 26, 2026

Triethylamine → 7-Bromo-6-methoxy-1(2H)-isoquinolinone

https://huagongshe.com/reaction/2060363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant4-Bromo-3-methoxycinnamic acidHCID 58005127—
SolventBenzeneHCID 241—
Product7-Bromo-6-methoxy-1(2H)-isoquinolinoneHCID 5800512559.9%

Reaction Steps

A portion of the product from Step 1 [(2E)-3-(4-bromo-3-methoxyphenyl)acrylic acid](12.5 g, 48.6 mmol) was azeotroped with benzene and suspended in benzene (94 mL). Triethylamine (9.49 mL, 68.1 mmol) and diphenylphosphoryl azide (10.48 mL, 48.6 mmol) were added and the reaction mixture stirred at RT for 1 h. The mixture was filtered through a pad of silica and eluted with ˜1 L of toluene, the volatiles evaporated, the residue resuspended in diphenylmethane (94 mL) and the mixture heated to reflux for three hours (internal temperature 250° C.). The reaction mixture was allowed to cool to RT, stirred overnight, filtered and the solid washed with hexanes (100 mL) to give tan solid (7.4 g). LRMS ESI+ (M+H)+ 254.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278322B2
Source datasetuspto-grants-2012_10
ORD IDord-303eae82c25440e5b034011d6793065f
Source noteuspto-grants-2012_10