HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1-Dimethylethyl (2S)-2-(phenylmethyl)-1-piperazinecarboxylate → (S)-5-(3-benzylpiperazin-1-yl)-3-cyclobutyl-1-methyl-1H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1-Dimethylethyl (2S)-2-(phenylmethyl)-1-piperazinecarboxylate | HCID 17750441 | — |
| Reactant | 5-Bromo-3-cyclobutyl-1-methyl-1H-indazole | HCID 58188999 | — |
| Product | (S)-5-(3-benzylpiperazin-1-yl)-3-cyclobutyl-1-methyl-1H-indazole | HCID 58189168 | 99% |
Reaction Steps
The title compound was prepared by the method outlined for Example 1 using 5-Bromo-3-cyclobutyl-1-methyl-1H-indazole as the aryl halide and (S)-2-benzyl-piperazine-1-carboxylic acid tert-butyl ester as the amine component to afford the title compound as a brown oil (409 mg, 99%). 1H NMR (MeOH-d4) 8.72 (d, J=8.7 Hz, 1H), 7.79 (d, J=8.8 Hz, 1H), 7.32-7.18 (m, 6H), 4.08 (s, 3H), 3.79-3.46 (m, 3H), 3.35-3.34 (m, 1H), 3.31-3.30 (m, 2H), 3.15-3.07 (m, 4H), 2.88-2.77 (m, 5H), 2.69-2.61 (m, 1H). LC/MS (Method B) 2.49 min, [M+1]+ 361.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08927546B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-e16e87e0e4524d32aaaa33b8d404daa4 |
| Source note | uspto-grants-2015_01 |