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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930304Generated: October 29, 2026

4,7-Dichloropyrido[3,2-d]pyrimidine → (4S,6S)-4-(5-((7-chloropyrido[3,2-d]pyrimidin-4-yl)amino)-2-fluoropyridin-3-yl)-4-methyl-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-amine

https://huagongshe.com/reaction/930304

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,7-Dichloropyrido[3,2-d]pyrimidineHCID 71428445—
ReactantN-(5-((4S,6S)-2-amino-4-methyl-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-4-yl)-6-fluoropyridin-3-yl)-5-chloropicolinamideHCID 78321763—
Product(4S,6S)-4-(5-((7-chloropyrido[3,2-d]pyrimidin-4-yl)amino)-2-fluoropyridin-3-yl)-4-methyl-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-amineHCID 78320811—

Reaction Steps

The title compound was synthesized using steps and procedures analogous to those described in Method B (step 2) above, but using (4S,6S)-4-(5-amino-2-fluoropyridin-3-yl)-4-methyl-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-amine (6a) and 4,7-dichloropyrido[3,2-d]pyrimidine (intermediate 9). MS m/z=456.0 [M+H]+. Calculated for C18H14ClF4N7O: 455.8

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296734B2
Source datasetuspto-grants-2016_03
ORD IDord-85aebccf54994e4ba22888477a9d287f
Source noteuspto-grants-2016_03