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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056715Generated: October 29, 2026

(S)-2-isobutyl-1-(2,2,2-trifluoroethyl)piperazine → 3-Amino-5-(6-((S)-3-isobutyl-4-(2,2,2-trifluoroethyl)piperazin-1-yl)-2-((S)-1-methoxypropan-2-ylamino)pyrimidin-4-yloxy)quinoxalin-2(1H)-one

https://huagongshe.com/reaction/2056715

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-2-isobutyl-1-(2,2,2-trifluoroethyl)piperazineHCID 58612005—
Reactant(S)-3-amino-5-(6-chloro-2-(1-methoxypropan-2-ylamino)pyrimidin-4-yloxy)quinoxalin-2(1H)-oneHCID 58612053—
Product3-Amino-5-(6-((S)-3-isobutyl-4-(2,2,2-trifluoroethyl)piperazin-1-yl)-2-((S)-1-methoxypropan-2-ylamino)pyrimidin-4-yloxy)quinoxalin-2(1H)-oneHCID 11635469—

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)-2-isobutyl-1-(2,2,2-trifluoroethyl)piperazine (89 mg, 0.4 mmol) under the conditions of Example 34 provided the title compound as an amorphous solid. MS (ESI, pos. ion) m/z: 565 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335672B2
Source datasetuspto-grants-2008_02
ORD IDord-3dc15a5fa0ac417f9abb1778dac6ffff
Source noteuspto-grants-2008_02