Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528053Generated: October 29, 2026

Triethylamine → HCID 86711715, compound

https://huagongshe.com/reaction/528053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant6-Chloro-N-methyl-5-nitro-4-pyrimidinamineHCID 2779167—
ReactantSpiro(indole-3,4'-piperidin)-2(1H)-oneHCID 18435788—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 86711715HCID 86711715—

Reaction Steps

A stirred solution of 6-chloro-N-methyl-5-nitropyrimidin-4-amine (1.0 g, 5.3 mmol) in methanol (20 mL) was added triethylamine (2.0 mL, 14.3 mmol) and spiro[indoline-3,4′-piperidin]-2-one (1072.5 mg, 5.3 mmol). The mixture was stirred at ambient temperature for 2 h and then 10 wt % Pd on C (wet) was added. The resulting mixture was stirred under hydrogen for 18 hours, diluted with methanol, and was filtered through Celite. The filtrate was concentrated, and the resulting solid was triturated with a solution of 50% aqueous methanol. The methanol was removed in vacuo and the mixture was filtered and dried under reduced pressure. The resulting compound was submitted to next step without further purification. 1H NMR (400 MHz, DMSO-d6) δ 10.39 (s, 1H), 7.86 (s, 1H), 7.45 (d, 1H), 7.20 (td, 1H), 6.98 (t, 1H), 6.87 (d, 1H), 6.30 (q, 1H), 4.15 (s, 2H), 3.45 (dd, 2H), 3.26-3.18 (m, 2H), 2.86 (d, 3H), 1.97-1.88 (m, 2H), 1.82 (dd, 2H). MS (EI) for C14H20N6O: 325.6 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346807B2
Source datasetuspto-grants-2016_05
ORD IDord-7fba7db63de94ed2b4015372e264aa3f
Source noteuspto-grants-2016_05