HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylcyclohexylamine → HCID 46834395, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylcyclohexylamine | HCID 7514 | — |
| Reactant | HCID 59490197 | HCID 59490197 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 46834395 | HCID 46834395 | — |
Reaction Steps
This was synthesized by using (S)-4-(6-(4-fluorophenyl)-5,6-dihydrobenzo[h]quinazolin-2-ylamino)phenethyl methanesulfonate, N-methylcyclohexanamine and triethylamine as described in general procedure 2 to afford the desired product. M.p.=160-162° C. 1H NMR (DMSO-d6) 400 MHz δ 10.37 (brs, 1H), 9.68 (s, 1H), 8.32-8.36 (m, 2H), 7.80 (d, J=7.8 Hz, 2H), 7.50-7.52 (m, 2H), 7.26 (d, J=8.2 Hz, 2H), 7.10-7.17 (m, 4H), 4.43 (t, J=6.6 Hz, 1H), 3.27-3.30 (m, 5H), 3.01-3.13 (m, 2H), 2.73 (d, J=4.6 Hz, 3H), 2.03-2.09 (m, 2H), 1.99 (s, 1H), 1.81 (d, J=12.1 Hz, 2H), 1.61 (d, J=12.5 Hz, 1H), 1.40-1.44 (m, 3H), 1.27-1.32 (m, 3H), 1.09-1.17 (m, 2H). LCMS m/e 507 [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08357694B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-7eda85f6afe64255be3d3db8af750f2c |
| Source note | uspto-grants-2013_01 |