HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,3-Diphenylpropylamine → 3-(5-chloro-4-(4-(methylsulfonyl)phenyl)thiazol-2-yl)-1-(3,3-diphenylpropyl)-1-(2-(tetrahydro-2H-pyran-4-yl)ethyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,3-Diphenylpropylamine | HCID 79698 | — |
| Reactant | 4-(2-Bromoethyl)oxane | HCID 22637012 | — |
| Reactant | 3,3-diphenyl-N-(2-(tetrahydro-2H-pyran-4-yl)ethyl)propan-1-amine | HCID 57586384 | — |
| Reactant | 5-Chloro-4-(4-(methylsulfonyl)phenyl)thiazol-2-amine | HCID 86628127 | — |
| Product | 3-(5-chloro-4-(4-(methylsulfonyl)phenyl)thiazol-2-yl)-1-(3,3-diphenylpropyl)-1-(2-(tetrahydro-2H-pyran-4-yl)ethyl)urea | HCID 57586359 | — |
| Product | 3,3-diphenyl-N-(2-(tetrahydro-2H-pyran-4-yl)ethyl)propan-1-amine | HCID 57586384 | — |
Reaction Steps
Compound 206 was prepared according to Method D using 5-chloro-4-(4-(methylsulfonyl)phenyl)thiazol-2-amine instead of N-(4-(2-amino-5-chlorothiazol-4-yl)phenyl)methanesulfonamide and 3,3-diphenyl-N-(2-(tetrahydro-2H-pyran-4-yl)ethyl)propan-1-amine instead of N-methyl-3,3-diphenylpropan-1-amine. 3,3-diphenyl-N-(2-(tetrahydro-2H-pyran-4-yl)ethyl)propan-1-amine was prepared according to Method C using 3,3-diphenylpropan-1-amine instead of tert-butyl 4-(2-aminoethyl)piperidine-1-carboxylate and 4-(2-bromoethyl)-tetrahydro-2H-pyran instead of 3-bromo-1,1-diphenylpropane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08324396B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-a0d8a02800074f47984fdaa4a9ab8312 |
| Source note | uspto-grants-2012_12 |