HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine hydrochloride → HCID 57979848, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | HCID 69048108 | HCID 69048108 | — |
| Product | HCID 57979848 | HCID 57979848 | — |
Reaction Steps
3-[({4-[(3-Chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl}methyl)(methyl)amino]piperidine-3-carboxylic acid (Isomer 1) was coupled with methylamine hydrochloride using an analogous method to that described for the equivalent step in Example 20 to give 3-[({4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl}methyl)(methyl)amino]-N-methylpiperidine-3-carboxamide (Example 89.1 Isomer 1); 1H NMR Spectrum: (DMSO d6) 1.43 (m, 1H); 1.66 (m, 1H); 1.84 (m, 1H); 2.11 (m, 1H); 2.29 (s, 3H); 2.58 (m, 1H); 2.73 (d, 3H); 2.84 (m, 2H); 3.28 (d, 1H); 3.69 (d, 1H); 3.78 (d, 1H); 4.00 (s, 3H); 7.24 (s, 1H); 7.35 (t, 1H); 7.56 (t, 1H); 7.64 (t, 1H); 7.79 (m, 1H); 8.37 (s, 1H); 8.48 (s, 1H); 9.75 (s, 1H); Mass Spectrum: (M+H)+ 487.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07632840B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-89587b342439439eb6f0509481673ddc |
| Source note | uspto-grants-2009_12 |