HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Chloromethyl)benzoyl chloride → N-[2-methyl-5-(3-morpholinobenzamido)phenyl]-3-chloromethylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Chloromethyl)benzoyl chloride | HCID 2733324 | — |
| Reactant | N-(3-amino-4-methylphenyl)-3-morpholinobenzamide | HCID 11301391 | — |
| Product | N-[2-methyl-5-(3-morpholinobenzamido)phenyl]-3-chloromethylbenzamide | HCID 22291061 | 98% |
Reaction Steps
Using an analogous procedure to that described in Example 63, 3-chloromethylbenzoyl chloride was reacted with N-(3-amino-4-methylphenyl)-3-morpholinobenzamide. There was thus obtained the title compound in 98% yield; NMR Spectrum: (DMSOd6) 2.19 (s, 3H), 3.17 (m, 4H), 3.75 (m, 4H), 4.85 (s, 2H), 7.13 (d, 1H), 7.22 (d, 1H), 7.34 (m, 2H), 7.44 (s, 1H), 7.54 (m, 2H), 7.65 (d, 1H), 7.79 (s, 1H), 7.95 (d, 1H). 8.03 (s, 1H), 9.96 (s, 1H), 10.12 (s, 1H); Mass Spectrum: M+H+ 464.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06956037B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-5b5db5023b5247f29e9b6365350ac1fa |
| Source note | uspto-grants-2005_10 |