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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661935Generated: November 2, 2026

1,2-Dichloroethane → HCID 59375067, compound

https://huagongshe.com/reaction/661935

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantGlycolic AcidHCID 757—
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 59375043HCID 59375043—
SolventAcetonitrile tetrahydrofuranHCID 22177404—
ProductHCID 59375067HCID 5937506760.7%

Reaction Steps

A solution of crude 7-(aminomethyl)-4-(2-methyl-3-(1-oxoisoindolin-2-yl)phenyl)-9H-carbazole-1-carboxamide (Example 33-1, 25 mg, 0.054 mmol), glycolic acid (8.26 mg, 0.109 mmol), HOAT (13.30 mg, 0.098 mmol), and EDC (20.81 mg, 0.109 mmol) in acetonitrile-THF (2:1) (5 mL) was treated with DIEA (0.028 mL, 0.163 mmol) and stirred at rt overnight. The mixture was concentrated and purified by preparative HPLC. The appropriate effluent fractions were concentrated to afford an aqueous suspension, which was treated with NaHCO3 (aq). The precipitate was collected by filtration, washed with water and dried to provide 7-((2-hydroxyacetamido)methyl)-4-(2-methyl-3-(1-oxoisoindolin-2-yl)phenyl)-9H-carbazole-1-carboxamide (17 mg, 59%). 1H NMR (400 MHz, DMSO-d6) δ 11.49 (1H, s), 8.22-8.28 (1H, m), 8.17 (1H, br. s.), 7.97-8.05 (1H, m), 7.81 (1H, d, J=7.5 Hz), 7.69 (2H, d, J=3.7 Hz), 7.54-7.66 (3H, m), 7.42-7.54 (2H, m), 7.28-7.38 (1H, m), 7.03 (1H, d, J=7.9 Hz), 6.94-7.00 (1H, m), 6.86-6.94 (1H, m), 5.45 (1H, br.), 4.88-5.05 (2H, m), 4.33-4.48 (2H, m), 3.88 (2H, s), 1.83 (3H, s). Mass spectrum m/z 519.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084620B2
Source datasetuspto-grants-2011_12
ORD IDord-81e73f05c7664320ada7ff3e027732e4
Source noteuspto-grants-2011_12