HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylcyclohexylamine → HCID 67540972, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylcyclohexylamine | HCID 7514 | — |
| Reactant | HCID 86645590 | HCID 86645590 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 67540972 | HCID 67540972 | — |
Reaction Steps
This was synthesized by using (S)-4-(6-(3,4-dichlorophenyl)-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.=175-185° C. 1H NMR 400 MHz (DMSO-d6) δ 10.54 (s, 1 H), 9.71 (s, 1 H), 8.33-8.28 (m, 2 H), 7.78-7.76 (m, 2 H), 7.51-7.42 (m, 3 H), 7.25-7.23 (m, 2 H), 7.11-7.10 (d, 1 H), 7.02-7.00 (m, 1 H), 4.46 (t, J=6.8 Hz, 1 H), 3.28-3.21 (m, 4 H), 3.00-2.98 (m, 2 H), 2.71-2.69 (d, 3 H), 2.09-1.96 (m, 2 H), 1.79 (d, J=12 Hz, 2 H), 1.59 (d, J=12.8 Hz, 2 H). 1.44-1.38 (m, 2 H), 1.26-1.06 (m, 4 H). LCMS m/e 557 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08357694B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-f32360d25e084d35925e6ab994d315c9 |
| Source note | uspto-grants-2013_01 |