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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225912Generated: November 2, 2026

1,2-Dichloroethane → HCID 6539891, compound

https://huagongshe.com/reaction/225912

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantWaterHCID 962—
ReactantAcrylic AcidHCID 6581—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactantmethyl((1-methyl-1H-indol-2-yl)methyl)amineHCID 11401058—
SolventDimethylformamideHCID 6228—
ProductHCID 6539891HCID 653989140%

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, 1 H), 8.59 (d, J=3.9 Hz, 1 H), 7.84 (d, J=7.6 Hz, 1 H), 7.76 (d, J=15.5 Hz, 1 H), 7.59 (d, J=7.8 Hz, 1 H), 7.38-7.48 (m, 2 H), 7.19-7.27 (m, 1 H), 7.08-7.17 (m, 1 H), 6.98 (d, J=15.5 Hz, 1 H), 6.51 (s, 1 H), 4.94 (s, 2 H), 3.73 (s, 3 H), 3.09 (s, 3 H); 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 numberUS07557125B2
Source datasetuspto-grants-2009_07
ORD IDord-e8e2915dcb844555a7d45b70cb9cc0c8
Source noteuspto-grants-2009_07