HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → (3-Chloro-4-(4-methylpiperazin-1-yl)phenyl)methanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 4-Amino-3,5-dichlorobenzylamine | HCID 18975763 | — |
| Reactant | Tert-butyl 3-chloro-4-(4-methylpiperazin-1-yl)benzylcarbamate | HCID 69058940 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3-Chloro-4-(4-methylpiperazin-1-yl)phenyl)methanamine | HCID 57887239 | — |
Reaction Steps
Step F (3): To a solution of tert-butyl 3-chloro-4-(4-methylpiperazin-1-yl)benzylcarbamate (36 mg, 0.1 mmol) from step F (2) in CH2Cl2 (0.5 mL) was added TFA (0.5 mmol). The mixture was stirred at rt for 2 h, and then the mixture was concentrated to give the title compound which was used without further purification. 1H-NMR (500 MHz, CD3OD) δ 7.59 (s, 1 H), 7.43 (d, J=8.24 Hz, 1 H), 7.27 (d, J=8.24 Hz, 1 H), 4.10 (s, 2 H), 3.60-3.70 (m, 2 H), 3.50-3.59 (m, 2 H), 3.29-3.42 (m, 2 H), 3.10-3.22 (m, 2 H), 2.98 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07601751B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-7dbeb1c906f549c6a258bff6663384d0 |
| Source note | uspto-grants-2009_10 |