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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842025Generated: October 31, 2026

Hydrochloric Acid → HCID 22617857, compound

https://huagongshe.com/reaction/842025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydro-4H-pyran-4-oneHCID 121599—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 22617879HCID 22617879—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 22617857HCID 2261785794%

Reaction Steps

To a stirred solution of N-[3-(2,6-dichloro-4-methoxy-phenyl)-2,5-dimethyl-pyrazolo[1,5-a]pyrimidin-7-yl]-ethane-1,2-diamine (3.32 g, 8.7 mmol) and tetrahydro-4H-pyran-4-one (1.8 g, 18 mmol) in methanol (60 mL)/acetic acid (1.6 g) was added sodium cyanoborohydride (1.1 g, 17 mmol), portionwise. After stirring 1 hour the reaction was concentrated under reduced pressure and then extracted from saturated aqueous sodium bicarbonate with ethyl acetate. The combined extracts were dried (Na2SO4), concentrated under reduced pressure to give the crude product as a colorless foam (4.1 g, quant). A solution of the product in ether (150 mL) was treated with 1 M ethereal HCl which generated a precipitate that was collected by vacuum filtration to give the title compound (4.1 g, 94%) as a pink solid: +APcI MS (M+1)+464; 1H NMR (methanol-d4) δ: 7.14 (s, 2H), 6.38 (s, 1H), 4.03 (dd, 2H), 3.94 (br t, 2H), 3.86 (s, 3H), 3.50-3.38 (m, 5H), 2.51 (s, 3H), 2.26 (s, 3H), 2.05 (m, 2H), 1.68 (qd, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372743B1
Source datasetuspto-grants-2002_04
ORD IDord-e7332dcca079459baa7410deb26c850a
Source noteuspto-grants-2002_04