HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(aminomethyl)-N,N-dimethylcyclobutan-1-amine → 4-{[4-Amino-5-(2,6-difluorobenzoyl)-1,3-thiazol-2-yl]amino}-N-{[1-(dimethylamino)cyclobutyl]methyl}benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(aminomethyl)-N,N-dimethylcyclobutan-1-amine | HCID 10606763 | — |
| Reactant | 4-[4-Amino-5-(2,6-difluoro-benzoyl)-thiazol-2-ylamino]-benzoic Acid | HCID 11257352 | — |
| Product | 4-{[4-Amino-5-(2,6-difluorobenzoyl)-1,3-thiazol-2-yl]amino}-N-{[1-(dimethylamino)cyclobutyl]methyl}benzamide | HCID 22731041 | 61% |
Reaction Steps
The title compound was prepared in a manner similar to Step 3 in Method A; from coupling 4-[4-amino-5-(2,6-difluoro-benzoyl)-thiazol-2-ylamino]-benzoic acid (3) and 1-(aminomethyl)-N,N-dimethylcyclobutanamine (Yang et al., Eur. J. Med. Chem. 31, 231-239 (1996)) to afford a yellow amorphous powder in 61% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06720346B2 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-51dda9a39e9a478ea1deb9225490c9aa |
| Source note | uspto-grants-2004_04 |