Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811104Generated: November 2, 2026

1,2-Dichloroethane → HCID 59375039, compound

https://huagongshe.com/reaction/1811104

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantAmmonium HydroxideHCID 14923—
ReactantHOAtHCID 181649—
ReactantHCID 59375149HCID 59375149—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59375039HCID 5937503932.2%

Reaction Steps

A mixture of 8-carbamoyl-5-(3-(4-fluorobenzamido)-2-methylphenyl)-9H-carbazole-2-carboxylic acid (Example 23-1, 30 mg, 0.062 mmol) and HOAT (12.72 mg, 0.093 mmol) in THF (0.4 mL) was treated with 28% aqueous ammonium hydroxide (0.052 mL, 0.374 mmol) and EDC (23.89 mg, 0.125 mmol) and the mixture was stirred at rt. After 22.5 h, the mixture was concentrated and purified by preparative HPLC. The appropriate effluent fractions were concentrated and the residue was treated with NaHCO3 (aq) and extracted three times with EtOAc. The combined organic phases were dried and concentrated to provide 4-(3-(4-fluorobenzamido)-2-methylphenyl)-9H-carbazole-1,7-dicarboxamide as an off-white solid (9.6 mg, 29%). 1H NMR (400 MHz, methanol-d4) δ 8.11 (d, J=1.3 Hz, 1 H) 8.03-8.08 (m, 2 H) 8.01 (d, J=7.9 Hz, 1 H) 7.51-7.55 (m, 1 H) 7.41-7.48 (m, 2 H) 7.29 (dd, J=7.5, 1.3 Hz, 1 H) 7.24 (t, J=8.8 Hz, 2 H) 7.08-7.12 (m, 2 H) 1.98 (s, 3 H). Mass spectrum m/z 481.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362065B2
Source datasetuspto-grants-2013_01
ORD IDord-c101b8bbb80140c79fdf61b736e314f2
Source noteuspto-grants-2013_01