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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567322Generated: October 30, 2026

Methyl bromoacetate → {9-[(3-Iodophenyl)methyl]-5-carbamoylcarbazol-4-yl}oxyacetic acid, methyl ester

https://huagongshe.com/reaction/567322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl bromoacetateHCID 60984—
ReactantHCID 22740042HCID 22740042—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product{9-[(3-Iodophenyl)methyl]-5-carbamoylcarbazol-4-yl}oxyacetic acid, methyl esterHCID 8675627386%

Reaction Steps

40% Methanolic Triton B (0.07 mL, 0.15 mM) was added to a solution of the 9-[(3-iodophenyl)methyl]-4-hydroxy-5-carbamoyl carbazole (60 mg, 0.13 mM) in 8 mL DMF at room temperature. After 3 minutes, methyl bromoacetate (30 mg, 0.19 mM) was added and the resultant mixture stirred at room temperature for 17 hours. The mixture was diluted with ethyl acetate, washed with H2O and saturated brine, dried over magnesium sulfate, filtered, and concentrated. The residue was purified by column chromatography on silica gel (elution with ethyl acetate) to afford 60 mg (86%) of the {9-[(3-iodophenyl)methyl]-5-carbamoylcarbazol-4-yl}oxyacetic acid, methyl ester as a white solid. 1H NMR (DMSO-d6) δ 7.6-7.0 (m, 11H), 6.6 (d, 1H, J=8 Hz), 5.7 (s, 2H), 4.9 (s, 2H), and 3.75 (s, 3H). IR (KBr, cm−1) 3500, 3350, 1727, 1642, 1291, 1236, and 772. MS (ES) m/e 515.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177440B1
Source datasetuspto-grants-2001_01
ORD IDord-bd426cddf8cf4c7094039a85fd529047
Source noteuspto-grants-2001_01