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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409154Generated: October 27, 2026

(S)-2-amino-6-(5-amino-2-fluoro-phenyl)-3,5,5,6-tetramethyl-5,6-dihydro-3H-pyrimidin-4-one → (6S)-2-amino-6-(5-(3-chloro-6,7-dihydro-5H-cyclopenta[b]pyridin-7-ylamino)-2-fluorophenyl)-3,5,5,6-tetramethyl-5,6-dihydropyrimidin-4(3H)-one

https://huagongshe.com/reaction/2409154

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-2-amino-6-(5-amino-2-fluoro-phenyl)-3,5,5,6-tetramethyl-5,6-dihydro-3H-pyrimidin-4-oneHCID 57497157—
ReactantHCID 58082858HCID 58082858—
ReactantHCID 178419135HCID 178419135—
Product(6S)-2-amino-6-(5-(3-chloro-6,7-dihydro-5H-cyclopenta[b]pyridin-7-ylamino)-2-fluorophenyl)-3,5,5,6-tetramethyl-5,6-dihydropyrimidin-4(3H)-oneHCID 56654776—

Reaction Steps

The reductive amination of (S)-2-amino-6-(5-amino-2-fluoro-phenyl)-3,5,5,6-tetramethyl-5,6-dihydro-3H-pyrimidin-4-one (intermediate J) and 3-chloro-5H-cyclopentapyridin-7(6H)-one using decaborane yielded (6S)-2-amino-6-(5-(3-chloro-6,7-dihydro-5H-cyclopenta[b]pyridin-7-ylamino)-2-fluorophenyl)-3,5,5,6-tetramethyl-5,6-dihydropyrimidin-4(3H)-one as a white foam. MS (ESI): m/z=430.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815881B2
Source datasetuspto-grants-2014_08
ORD IDord-7d85bfc46f214c6d90c338d110c91295
Source noteuspto-grants-2014_08