HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 11242947, compound → HCID 11291280, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 11242947 | HCID 11242947 | — |
| Reactant | HCID 57518307 | HCID 57518307 | — |
| Product | HCID 11291280 | HCID 11291280 | 65% |
Reaction Steps
The title compound was prepared in 65% yield from 2-(2,5-dichloro-6-oxo-6H-pyrimidin-1-ylmethyl)-benzonitrile (Example 15B) and (R)-3-methyl-piperidin-3-ylamine according to the general procedure outlined for Example 1 and was isolated as the HCl salt. 1H NMR (400 MHz, DMSO-d6): δ 8.43 (br s, 3H), 8.09 (s, 1H), 7.80 (d, 1H, J=7.6 Hz), 7.64 (t, 1H, J=7.6 Hz), 7.45 (t, 1H, J=7.6 Hz), 7.22 (d, 1H, J=7.6 Hz), 5.39 (AB q, 2H, J=98.0, 14.8 Hz), 3.39-3.47 (m, 1H), 3.01-3.15 (m, 2H), 2.80-2.90 (m, 1H), 1.81-2.00 (m, 2H), 1.56-1.66 (m, 2H), 1.30 (m, 3H). MS (ES) [m+H] calc'd for C18H20N5OCl, 358, 360; found 358, 360.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07470700B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-75088f9624404c3aaaa2beda029ab2da |
| Source note | uspto-grants-2008_12 |