HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(3-Iodopropyl)-4-(5-phenoxypentyl)benzene → Methyl 3-({[3-(methoxycarbonyl)cyclohexyl]amino}carbonyl)-4-{3-[4-(5-phenoxy-pentyl)phenyl]propoxy}benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(3-Iodopropyl)-4-(5-phenoxypentyl)benzene | HCID 57589112 | — |
| Reactant | Methyl 4-hydroxy-3-({[3-(methoxycarbonyl)cyclohexyl]amino}carbonyl)benzoate | HCID 57589182 | — |
| Product | Methyl 3-({[3-(methoxycarbonyl)cyclohexyl]amino}carbonyl)-4-{3-[4-(5-phenoxy-pentyl)phenyl]propoxy}benzoate | HCID 57589216 | — |
Reaction Steps
Preparation takes place in analogy to Example 22 from the (+)-B-enantiomer of methyl 4-hydroxy-3-({[3-(methoxycarbonyl)cyclohexyl]amino}carbonyl)benzoate (see Example IX, method 2) and 1-(3-iodopropyl)-4-(5-phenoxypentyl)benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07498460B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-985b55b181f14481821c27b015ed89ad |
| Source note | uspto-grants-2009_03 |