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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503479Generated: October 30, 2026

2-Chloro-N-methyl-5-(trifluoromethyl)pyrimidin-4-amine → 2-N-(6,6-dimethyl-4,7-dihydropyrazolo[5,1-c][1,4]oxazin-3-yl)-4-N-methyl-5-(trifluoromethyl)pyrimidine-2,4-diamine

https://huagongshe.com/reaction/1503479

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-N-methyl-5-(trifluoromethyl)pyrimidin-4-amineHCID 21077587—
Reactant6,6-dimethyl-6,7-dihydro-4H-pyrazolo[5,1-c][1,4]oxazin-3-amineHCID 90010421—
Solventtert-ButanolHCID 6386—
Product2-N-(6,6-dimethyl-4,7-dihydropyrazolo[5,1-c][1,4]oxazin-3-yl)-4-N-methyl-5-(trifluoromethyl)pyrimidine-2,4-diamineHCID 7220148936%

Reaction Conditions

Temperature100 °C

Reaction Steps

A microwave vial equipped with a magnetic stirrer was charged with 6,6-dimethyl-6,7-dihydro-4H-pyrazolo[5,1-c][1,4]oxazin-3-amine (13 mg, 0.078 mmol), 2-chloro-N-methyl-5-(trifluoromethyl)pyrimidin-4-amine (20 mg, 0.095 mmol), and t-BuOH (0.5 mL). The mixture was heated at 100° C. under microwave irradiation for 15 min. After concentration, the residue was purified by prep-HPLC to give the title compound (9.5 mg, 36%). 1H NMR (500 MHz, CDCl3) δ 8.09 (s, 1H), 7.67 (s, 1H), 6.79 (s, 1H), 5.18 (s, 1H), 4.83 (s, 2H), 3.93 (s, 2H), 3.00 (d, J=4.5 Hz, 3H), 1.63 (s, 6H). LC-MS (Method B): m/z=343.3 (M+H)+, 4.77 min, 98.2% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212186B2
Source datasetuspto-grants-2015_12
ORD IDord-61752ca0b37e49aca396469ac48d660d
Source noteuspto-grants-2015_12