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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761110Generated: November 3, 2026

1,2-Dichloroethane → HCID 6539891, compound

https://huagongshe.com/reaction/1761110

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactanttrans-3-(3-Pyridyl)acrylic acidHCID 776396—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactantmethyl((1-methyl-1H-indol-2-yl)methyl)amineHCID 11401058—
SolventDimethylformamideHCID 6228—
ProductHCID 6539891HCID 653989140.2%

Reaction Steps

EDC (0.22 g, 1.14 mmole) was added to a solution of trans-3-(3-pyridyl)acrylic acid (0.17 g, 1.14 mmole), 1-methyl-2-(methylaminomethyl)-1H-indole (0.20 g, 1.15 mmole), and HOBt H2O (0.15 g, 1.11 mmole) in DMF (10 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 (0.14 g, 40%) as a white solid: 1H NMR (360 MHz, CDCl3) indicated an approximately 8:1 mixture of amide rotamers; for the major rotamer: δ 8.79 (s,1H), 8.59 (d, J=3.9 Hz,1H), 7.84 (d, J=7.6 Hz,1H), 7.76 (d, J=15.5 Hz,1H), 7.59 (d, =7.8 Hz,1H), 7.38-7.48 (m, 2H), 7.19-7.27 (m,1H), 7.08-7.17 (m,1H), 6.98 (d,J=15.5 Hz,1H), 6.51 (s,1H), 4.94 (s, 2H), 3.73 (s, 3H), 3.09 (s, 3H); MS (ES) m/e 306 (M+H)+. Anal. Calcd for C19H19N3O 0.20H2O: C, 73.86; H. 6.33; N, 13.60. Found: C, 73.52; H. 6.32; N. 13.43.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06846819B1
Source datasetuspto-grants-2005_01
ORD IDord-20bd98ddd23246159b15e6bb3e47fb12
Source noteuspto-grants-2005_01