HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → (4-Aminomethyl-benzyl)-(1H-benzimidazol-2-ylmethyl)(5,6,7,8-tetrahydro-quinolin-7-yl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-{[[4-(tert-Butoxycarbonylamino-methyl)-benzyl]-(5,6,7,8-tetrahydro-quinolin-7-yl)-amino]-methyl}-benzimidazole-1-carboxylic acid tert-butyl ester | HCID 68901448 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4-Aminomethyl-benzyl)-(1H-benzimidazol-2-ylmethyl)(5,6,7,8-tetrahydro-quinolin-7-yl)-amine | HCID 22601338 | 89.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06835731B2 |
| Source dataset | uspto-grants-2004_12 |
| ORD ID | ord-e50f6acbd442478cbda60d90e282664c |
| Source note | uspto-grants-2004_12 |