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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723989Generated: October 30, 2026

Bicarbonate Ion → HCID 10115879, compound

https://huagongshe.com/reaction/723989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBicarbonate IonHCID 769—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 10110826HCID 10110826—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 10115879HCID 1011587950%

Reaction Steps

To a solution of 3-[2-(cyclopentylamino)-4-pyrimidinyl]-2-(4-fluorophenyl)pyrazolo[1,5-α]pyridin-5-amine (60 mg, 0.15 mmol) in anhydrous pyridine (5 mL) was added methylsulfonyl chloride (36 mg, 0.3 mmol). The reaction was stirred at room temperature overnight. The reaction mixture was diluted with ethyl acetate, then saturated aquous bicarbonate was added. The phases were separated, the organic phase was washed with water, brine and dried (magnesium sulfate). Filtration and concentration, followed by flash chromatography (1:1 ethyl acetate-hexane) gave N-[3-[2-(cyclopentylamino)-4-pyrimidinyl]-2-(4-fluorophenyl)pyrazolo[1,5-α]pyridin-5-yl]methanesulfonamide (35 mg, 50%) as a solid. 1H-NMR (CDCl3): δ 8.42 (d, 1H), 8.15 (d, 1H), 8.05 (d, 1H), 7.60 (q, 2H), 7.13 (t, 2H), 6.90 (dd, 1H), 6.30 (d, 1H), 5.34 (d, 1H), 4.30 (m, 1H), 3.12 (s, 3H), 1.5–2.2 (m, 8H); 19F-NMR (CDCl3): δ −112.64; MS m/z 467 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141569B2
Source datasetuspto-grants-2006_11
ORD IDord-ee47b192f7044a6aa1d12ccd91ba9914
Source noteuspto-grants-2006_11