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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581685Generated: October 30, 2026

1,2-Dichloroethane → HCID 9798694, compound

https://huagongshe.com/reaction/1581685

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantWaterHCID 962—
Reactanto-Phenylbenzoic acidHCID 70357—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactantmethyl((1-methyl-1H-indol-2-yl)methyl)amineHCID 11401058—
SolventDimethylformamideHCID 6228—
ProductHCID 9798694HCID 979869425%

Reaction Steps

EDC (0.22 g, 1.14 mmole) was added to a solution of 2-biphenylcarboxylic acid (0.22 g, 1.14 mmole), 1-methyl-2-(methylaminomethyl)indole (0.20 g, 1.15 mmole), and HOBt.H2O (0.15 g, 1.11 mmole) in DMF (20 mL) at RT. The reaction was stirred overnight, then was concentrated in vacuo. The residue was diluted with 5% NaHCO3 and extracted with CH2Cl2. The combined organic extracts were washed with brine and dried over MgSO4. Flash chromatography on silica gel (3% MeOH/CH2Cl2) followed by preparative TLC (3% MeOH/CH2Cl2) gave the title compound (0.10 g, 25%) as a light yellow solid: 1H NMR (360 MHz, CDCl3) indicated an approximately 5:1 mixture of amide rotamers; for the major rotamer: δ 7.03-7.58 (m, 13H), 6.19 (s, 1H), 4.50 -5.00 (m, 2H), 3.57 (s, 3H), 2.40 (s, 3H); for the minor rotamer: δ 7.03-7.58 (m, 13H), 6.14 (s, 1H), 4.50-5.00 (m, 2H), 3.38 (s, 3H), 2.76 (s, 3H); MS (ES) m/e 356 (M+H)+. Anal. Calcd for C24H22N2O.0.80H2O: C, 78.15; H, 6.45; N, 7.59. Found: C, 77.96; H, 6.29; N, 7.35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730684B1
Source datasetuspto-grants-2004_05
ORD IDord-0af47ba5b8734d2e9434bb4f573281ea
Source noteuspto-grants-2004_05