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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921046Generated: October 30, 2026

1,2-Dichloroethane → HCID 22593808, compound

https://huagongshe.com/reaction/1921046

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(2E)-3-(6-aminopyridin-3-yl)prop-2-enoic acidHCID 10487224—
ReactantHCID 22593742HCID 22593742—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 22593808HCID 2259380842.2%

Reaction Steps

EDC (230 mg, 1.2 mmole) was added to a solution (E)-3-(6-aminopyridin-3-yl)acrylic acid (164 mg, 1.0 mmole), 2-(methylaminomethyl)thieno[3,2-b]thiophene (220 mg, 1.2 mmole), HOBt.H2O (162 mg, 1.2 mmole), and Et3N (0.35 mL, 2.5 mmole) in dry DMF (5 mL) at RT. After 18 hr the mixture was diluted with H2O and extracted with EtOAc (3×). The combined organic layers were dried (MgSO4) and concentrated. The solid was taken up in 1:1 MeOH/H2O and filtered. The filtrate was concentrated to approximately ⅓ volume. The precipitate was collected by filtration, washed with H2O, and dried in vacuo to afford the title compound (139 mg, 42%) as a light tan solid: 1H NMR (400 MHz, d6-DMSO) δ 8.15 (d, J=2.0 Hz, 1H), 7.83 (bd. 1H), 7.61 (d, J=5.2 Hz, 1H), 7.40 (m, 3H); 6.45 (m, 2H), 4.75 (s, 2H), 3.13 (s, 3H); for minor rotomer δ 5.00 (s, 2H), 2.95 (s, 3H); MS (ES) m/e 330 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173646B2
Source datasetuspto-grants-2012_05
ORD IDord-8f06f70a7c374befa451c476859a731f
Source noteuspto-grants-2012_05