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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244427Generated: October 26, 2026

Tris(hydroxymethyl)aminomethane → 7-methyl-2-Quinolinecarboxamide

https://huagongshe.com/reaction/1244427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(hydroxymethyl)aminomethaneHCID 6503—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(9H-Fluoren-9-yl)methyl 2-oxoethylcarbamateHCID 10858926—
Reactant7-Methylquinoline-2-carboxylic acidHCID 21919328—
SolventDichloromethaneHCID 6344—
Product7-methyl-2-QuinolinecarboxamideHCID 23532041339.2%

Reaction Steps

A solution of the amine 4 (1.0 mg, 1.9 μmol, 1.0 equiv) in dichloromethane (0.1 mL) was added to 7-methylquinoline-2-carboxylic acid (2.8 μmol, 1.5 equiv) and 1-hydroxybenzotriazole (0.44 mg, 3.2 μmol, 1.7 equiv) in a vial at 23° C. The solution was stirred for 5 min, then N-cyclohexylcarbodiimide-N′-propyloxymethyl polystyrene (Argonaut Technologies, 1.13 mmol/g, 3.4 mg, 3.8 μmol, 2.0 equiv) was added in one portion at 23° C. The reaction mixture was stirred gently at 23° C. under an argon atmosphere for 16 h. PS-Trisamine (Argonaut Technologies, 4.71 mmol/g, 2.0 mg, 9.5 μmol, 5.0 equiv) was then added in one portion and the reaction mixture was stirred for a further 2 h. The mixture was filtered through Celite (0.5 cm) and concentrated in vacuo to give the 7-methylquinoline-2-carboxylic acid amide derivative (1.2 mg, 95%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122549B2
Source datasetuspto-grants-2006_10
ORD IDord-995aca66a323444badc721d3f5a93460
Source noteuspto-grants-2006_10