HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Chloromethyl)benzoyl chloride → N-[5-(3-dimethylaminobenzamido)-2-methylphenyl]4-chloromethylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Chloromethyl)benzoyl chloride | HCID 70136 | — |
| Reactant | HCID 22057981 | HCID 22057981 | — |
| Product | N-[5-(3-dimethylaminobenzamido)-2-methylphenyl]4-chloromethylbenzamide | HCID 22291036 | — |
Reaction Steps
4-Chloromethylbenzoyl chloride was reacted with N-(3-amino-4-methylphenyl)-3-dimethylaminobenzamide using an analogous procedure to that described in Example 37 except that the reaction product was triturated under water rather than under 2N aqueous hydrochloric acid solution. There was thus obtained the title compound; NMR Spectrum: (DMSOd6) 2.19 (s, 3H), 2.95 (s, 6H), 4.28 (s, 2H), 6.9 (d, 1H), 7.21 (m, 3H), 7.29 (d, 1H), 7.58 (d, 3H), 7.8 (s, 1H), 7.96 (d, 2H), 9.9 (s, 1H), 10.08 (s, 1H); Mass Spectrum: M−H− 420.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06956037B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-9760db3b90f34f1d898c8177ec1a2202 |
| Source note | uspto-grants-2005_10 |