HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl (2S)-2-(2-methylpropyl)piperazine-1-carboxylate → (S)-tert-Butyl 4-(6-(3-amino-2-oxo-1,2-dihydroquinoxalin-5-yloxy)-2-((S)-1-methoxypropan-2-ylamino)pyrimidin-4-yl)-2-isobutylpiperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl (2S)-2-(2-methylpropyl)piperazine-1-carboxylate | HCID 17750437 | — |
| Reactant | (S)-3-amino-5-(6-chloro-2-(1-methoxypropan-2-ylamino)pyrimidin-4-yloxy)quinoxalin-2(1H)-one | HCID 58612053 | — |
| Product | (S)-tert-Butyl 4-(6-(3-amino-2-oxo-1,2-dihydroquinoxalin-5-yloxy)-2-((S)-1-methoxypropan-2-ylamino)pyrimidin-4-yl)-2-isobutylpiperazine-1-carboxylate | HCID 58612011 | — |
Reaction Steps
The reaction of (S)-3-amino-5-(6-chloro-2-(1-methoxypropan-2-ylamino)pyrimidin-4-yloxy)quinoxalin-2(1H)-one (74 mg, 0.2 mmol, Example 122(b)) with (S)-tert-butyl 2-isobutylpiperazine-1-carboxylate (48 mg, 0.2 mmol, CNH-Tech) under the conditions of Example 34 provided the title compound as an amorphous solid. MS (ESI, pos. ion) m/z: 583 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07335672B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-be4e70192b9241909c41a386d8ac5dd5 |
| Source note | uspto-grants-2008_02 |