HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(3-cyclopropyl-4-((4-methylpiperazin-1-yl)methyl)phenyl)-3-iodo-4-methylbenzamide → 3-[(2-amino-1,3-thiazol-5-yl)ethynyl]-N-{3-cyclopropyl-4-[(4-methylpiperazin-1-yl)methyl]phenyl}-methylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(3-cyclopropyl-4-((4-methylpiperazin-1-yl)methyl)phenyl)-3-iodo-4-methylbenzamide | HCID 46839047 | — |
| Reactant | Tert-butyl (5-ethynylthiazol-2-yl)carbamate | HCID 57737416 | — |
| Product | 3-[(2-amino-1,3-thiazol-5-yl)ethynyl]-N-{3-cyclopropyl-4-[(4-methylpiperazin-1-yl)methyl]phenyl}-methylbenzamide | HCID 86631107 | — |
Reaction Steps
The title compound can be synthesized from tert-butyl (5-ethynyl-1,3-thiazol-2-yl)carbamate and N-(3-cyclopropyl-4-((4-methylpiperazin-1-yl)methyl)phenyl)-3-iodo-4-methylbenzamide in a manner similar to that described for Example 2 (nitro reduction performed in a manner similar to that described for Example 8; 0.25M in MeOH/10% AcOH). T-BOC deprotection can be performed after coupling as described in Example 5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08278307B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-ef855e9658b54252b90c9469c9b718f3 |
| Source note | uspto-grants-2012_10 |