HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[2-(4-chloro-2-hydroxyphenyl)ethyl]acetamide → tert-Butyl 3-{2-[2-(2-acetylaminoethyl)-5-chlorophenoxy]ethoxy}-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[2-(4-chloro-2-hydroxyphenyl)ethyl]acetamide | HCID 68499121 | — |
| Reactant | Tert-butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-[2-(toluene-4-sulphonyloxy)ethoxy]piperidine-1-carboxylate | HCID 86609984 | — |
| Product | tert-Butyl 3-{2-[2-(2-acetylaminoethyl)-5-chlorophenoxy]ethoxy}-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylate | HCID 68500784 | — |
Reaction Steps
Analogously to Method G, 0.458 g of tert-butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-[2-(toluene-4-sulphonyloxy)ethoxy]piperidine-1-carboxylate (Example 14b) and 0.30 g of N-[2-(4-chloro-2-hydroxyphenyl)ethyl]acetamide are reacted. The title compound is obtained as a yellow oil. Rf=0.70 (EtOAc); Rt=5.75.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07790715B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-1f88e0b6aeb544b289f3d11da51757ee |
| Source note | uspto-grants-2010_09 |