HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylcyclohexylamine → HCID 54489262, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylcyclohexylamine | HCID 7514 | — |
| Reactant | 4-chloro-6-methyl-7H-pyrrolo[2,3-d]pyrimidine | HCID 335407 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 54489262 | HCID 54489262 | 58% |
Reaction Steps
The product from Method H (50 mg/0.298 mmol) was reacted with 100 mg (0.883 mmol) of N-methylcyclohexylamine as described in Method B. The reaction mixture was worked up as in Method B with the exception that ethyl acetate was used in place of ether. The title compound (42 mg, 58% yield) was obtained as a white solid. Mp 221° C. dec. 1H NMR (400 MHz, CDCl3) δ: 1.15-1.25 (m, 1H), 1.43-1.62 (m, 4H), 1.73 (br s, 1H, J=13.7 Hz), 1.82-1.90 (m, 4H), 2.41 (d, 3H, J=0.8 Hz), 3.21 (s, 3H) 4.63 (br s, 1H), 6.20 (s, 1H), 8.22 (s, 1H), 10.1 (br s, 1H). LRMS: 245 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06890929B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-fbf6e7abf1ae4c39ae5e2524a969b735 |
| Source note | uspto-grants-2005_05 |