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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056716Generated: October 31, 2026

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

https://huagongshe.com/reaction/2056716

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (2S)-2-(2-methylpropyl)piperazine-1-carboxylateHCID 17750437—
Reactant(S)-3-amino-5-(6-chloro-2-(1-methoxypropan-2-ylamino)pyrimidin-4-yloxy)quinoxalin-2(1H)-oneHCID 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-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335672B2
Source datasetuspto-grants-2008_02
ORD IDord-be4e70192b9241909c41a386d8ac5dd5
Source noteuspto-grants-2008_02