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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370141Generated: October 29, 2026

Diisopropylethylamine → HCID 58075815, compound

https://huagongshe.com/reaction/2370141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethylamine hydrochlorideHCID 6364545—
Reactant2,4-Dichloro-8-phenyl-7,8-dihydro-5H-pyrano[4,3-D]pyrimidineHCID 58075529—
SolventMethanolHCID 887—
ProductHCID 58075815HCID 5807581566.2%

Reaction Steps

To a solution of 2,4-dichloro-8-phenyl-7,8-dihydro-5H-pyrano[4,3-d]pyrimidine (Preparation I) (194 mg, 0.690 mmol) in MeOH (6901 μL) was added methanamine hydrochloride (69.9 mg, 1.035 mmol) and N,N-Diisopropylethylamine (301 μL, 1.725 mmol). The resulting mixture was stirred at RT for 2 h. The reaction mixture was then concentrated in vacuo. Purification by flash chromatography (Silica, EtOAc/Hexanes) gave 2-chloro-N-methyl-8-phenyl-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-amine (126 mg, 0.457 mmol, 66.2% yield). LC-MS (M+H)+=276.0. 1H NMR (500 MHz, CDCl3) δ ppm 7.28 (2 H, t, J=7.32 Hz), 7.20-7.25 (1 H, m), 7.14-7.20 (2 H, m), 4.47-4.62 (2 H, m), 4.47 (1 H, s), 4.00-4.11 (2 H, m), 3.95 (1 H, d, J=3.36 Hz), 3.08 (3 H, d, J=4.88 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710061B2
Source datasetuspto-grants-2014_04
ORD IDord-d532f28d14a4440d822a599111ce5482
Source noteuspto-grants-2014_04