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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723689Generated: November 2, 2026

N-Iodosuccinimide → 8-(2-chloro-4-iodophenylamino)-6,7-difluoro-4-methyl-2H-phthalazin-1-one

https://huagongshe.com/reaction/1723689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant8-(2-chlorophenylamino)-6,7-difluoro-4-methyl-2H-phthalazin-1-oneHCID 67404366—
SolventAcetic acid tetrahydrofuranHCID 23444217—
Product8-(2-chloro-4-iodophenylamino)-6,7-difluoro-4-methyl-2H-phthalazin-1-oneHCID 1135133618.5%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 8-(2-chlorophenylamino)-6,7-difluoro-4-methyl-2H-phthalazin-1-one (30 mg, 0.093 mmol) and NIS (24 mg, 0.11 mmol) in AcOH-THF (2 mL/0.5 mL) was heated at 85° C. for 3 minutes The reaction mixture was concentrated in vacuo and washed with water. The organic layer was dried over MgSO4, filtered, and concentrated in vacuo to give the crude material that was purified by silica gel flash column chromatography (100% hexanes to 15% EtOAc in hexanes) to afford 8-(2-chloro-4-iodophenylamino)-6,7-difluoro-4-methyl-2H-phthalazin-1-one (7.7 mg, 17%). MS APCI (−) m/z 446, 448 (M-, Cl pattern) detected; 1H NMR (400 MHz, DMSO-d6) δ 12.74 (s, 1H), 10.96 (s, 1H), 7.86 (s, 1H), 7.60 (d, 1H), 7.53 (dd, 1H), 6.94 (t, 1H), 2.47 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485643B2
Source datasetuspto-grants-2009_02
ORD IDord-0ed3e2cab4cf43da8664926eba466d1e
Source noteuspto-grants-2009_02