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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338612Generated: October 30, 2026

Hydrochloric Acid → HCID 67078752, compound

https://huagongshe.com/reaction/338612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Aminobenzoic AcidHCID 978—
ReactantTriethylamineHCID 8471—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantHCID 18952396HCID 18952396—
SolventAcetonitrileHCID 6342—
SolventSodium HydroxideHCID 14798—
ProductHCID 67078752HCID 6707875267.6%

Reaction Steps

Dissolving 3-pyridylacrylic acid (1.49 g, 10 mmol) and HBTU (3.79 g, 10 mmol) into 10 ml of acetonitrile, drop-adding triethylamine (2.02 g, 20 mmol), stirring at room temperature 30 minutes, to obtain a yellow sticky liquid. Dissolving p-aminobenzoic acid (1.52 g, 10 mmol) in 10 ml of 1 mol/L sodium hydroxide aqueous solution, and thereto drop-adding the above yellow sticky liquid at 60° C. After completion of drop-addition, maintaining the temperature for 1 hour to complete the reaction. The reaction solution is adjusted to pH of about 7 with concentrated hydrochloric acid. Large amount of solids are precipitated, filtrated and dried to obtain 1.90 g of 4-[(3-pyridylacryloyl)aminomethyl]benzoic acid (intermediate M-20) as a white solid, with a yield of 67.6%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889876B2
Source datasetuspto-grants-2014_11
ORD IDord-c0c404799020498c9171f27fbbb7454d
Source noteuspto-grants-2014_11