HuagongsheHuagongshe Chemistry Print Report · For research reference only
t-butyl(diphenyl)silyl 3-chloro-4-[(2S)oxiranylmethoxy]phenyl ether → 1-[4-(4-{[(2S)-3-(2-Chloro-4-hydroxy-phenoxy)-2-hydroxy-propylamino]-methyl}-piperidine-1-sulfonyl}-phenyl]-3-(2,5-difluoro-benzyl)-urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | t-butyl(diphenyl)silyl 3-chloro-4-[(2S)oxiranylmethoxy]phenyl ether | HCID 23381354 | — |
| Reactant | N-(4-{[4-(aminomethyl)-1-piperidinyl]sulfonyl}phenyl)-N'-(2,5-difluorobenzyl)urea formate | HCID 69999063 | — |
| Product | 1-[4-(4-{[(2S)-3-(2-Chloro-4-hydroxy-phenoxy)-2-hydroxy-propylamino]-methyl}-piperidine-1-sulfonyl}-phenyl]-3-(2,5-difluoro-benzyl)-urea | HCID 10146071 | 19.7% |
Reaction Steps
N-(4-{[4-(aminomethyl)-1-piperidinyl]sulfonyl}phenyl)-N′-(2,5-difluorobenzyl)urea formate (0.827 g, 1.72 mmol) was reacted with t-butyl(diphenyl)silyl 3-chloro-4-[(2S)oxiranylmethoxy]phenyl ether (0.516 9,1.17 mmol) according to example 37 to give the title compound (0.15 g, 0.23 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06506901B2 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-69df0de30f1f4ceda22eea21c050127f |
| Source note | uspto-grants-2003_01 |