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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842715Generated: November 4, 2026

Methanol → HCID 71240866, compound

https://huagongshe.com/reaction/1842715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant3-(2,5-Dichloropyrimidin-4-yl)pyrazolo[1,5-a]pyridineHCID 59291162—
Reactant2-methoxy-4-(1-methyl-3,6-dihydro-2H-pyridin-4-yl)-5-nitroanilineHCID 86677325—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71240866HCID 7124086672.1%

Reaction Steps

A mixture of 3-(2,5-dichloropyrimidin-4-yl)pyrazolo[1,5-a]pyridine (Intermediate 21, 575 mg, 1.86 mmol) and 2-methoxy-4-(1-methyl-3,6-dihydro-2H-pyridin-4-yl)-5-nitroaniline (Intermediate 3, 490 mg, 1.86 mmol) was stirred in THF (30 mL) and cooled in an ice/water bath. Lithium bis(trimethylsilyl)amide (4.10 mL, 4.10 mmol, 1M in THF) was then added dropwise and the mixture was stirred for 1 h. CH3OH was added and the mixture was concentrated in vacuo. The crude material was suspended in CH3OH and the mixture was filtered. The collected solid was washed with CH3OH and diethyl ether and dried on the filter to give the title compound (660 mg, 72%) as a yellow powder; 1H NMR: 2.29 (3H, s), 2.30-2.38 (2H, m), 2.58 (2H, t), 2.97 (2H, dd), 3.96 (3H, s), 5.60-5.68 (1H, m), 7.00 (1H, s), 7.16 (1H, td), 7.36-7.45 (1H, m), 8.49-8.56 (3H, m), 8.87 (1H, d), 8.90 (1H, s), 8.97 (1H, s); m/z: ES+ MH+ 492.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946235B2
Source datasetuspto-grants-2015_02
ORD IDord-a9ae075771974ec0b1d79ebe15e991bf
Source noteuspto-grants-2015_02