HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-4-isocyanato-1-(trifluoromethyl)benzene → HCID 52913369, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-4-isocyanato-1-(trifluoromethyl)benzene | HCID 14368497 | — |
| Reactant | HCID 67087051 | HCID 67087051 | — |
| Product | HCID 52913369 | HCID 52913369 | 88% |
Reaction Steps
In analogy to the procedure described in the second part of example 120 step E, (2S,5S)-1-[4-((S)-4-hydroxy-6-aza-spiro[2.5]oct-6-yl)-4-oxo-butyl]-5-methyl-6-oxo-piperazine-2-carboxylic acid amide was reacted with 2-chloro-4-isocyanato-1-trifluoromethyl-benzene (intermediate 16) to give the titled compound in 88% yield as a colorless solid. MS: 574.3 (MH+, 1Cl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08445674B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-35e9bf1d27894dc5ab0b233d6596e916 |
| Source note | uspto-grants-2013_05 |