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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308292Generated: October 26, 2026

Trifluoroacetic acid → (4-Aminomethyl-benzyl)-(1H-benzimidazol-2-ylmethyl)(5,6,7,8-tetrahydro-quinolin-7-yl)-amine

https://huagongshe.com/reaction/2308292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-{[[4-(tert-Butoxycarbonylamino-methyl)-benzyl]-(5,6,7,8-tetrahydro-quinolin-7-yl)-amino]-methyl}-benzimidazole-1-carboxylic acid tert-butyl esterHCID 68901448—
SolventDichloromethaneHCID 6344—
Product(4-Aminomethyl-benzyl)-(1H-benzimidazol-2-ylmethyl)(5,6,7,8-tetrahydro-quinolin-7-yl)-amineHCID 2260133889.3%

Reaction Steps

To a stirred solution of 2-{[[4-(tert-Butoxycarbonylamino-methyl)-benzyl]-(5,6,7,8-tetrahydro-quinolin-7-yl)-amino]-methyl}-benzimidazole-1-carboxylic acid tert-butyl ester (120 mg, 0.20 mmol) in anhydrous CH2Cl2 (1 mL) was added TFA (1 mL). The resultant solution was stirred at room temperature overnight. The mixture was concentrated in vacuo, dissolved with MeOH, and added NaHCO3. The mixture was stirred for 20 min, diluted with CH2Cl2, filtered through celite. The crude product was purified by flash chromatography on silica gel (2:2:96 CH3OH—NH3 H2O—CH2Cl2) afforded the title compound (71 mg, 89%) as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06835731B2
Source datasetuspto-grants-2004_12
ORD IDord-e50f6acbd442478cbda60d90e282664c
Source noteuspto-grants-2004_12