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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471539Generated: October 29, 2026

Hydrochloric Acid → HCID 57968770, compound

https://huagongshe.com/reaction/1471539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57968898HCID 57968898—
SolventMethanolHCID 887—
ProductHCID 57968770HCID 5796877032%

Reaction Steps

To a clear solution of 2-[3-formyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenoxy]-6-(2-methoxy-ethylamino)-nicotinonitrile (10) (440 mg, 1.04 mmol) in MeOH (anhydrous, 100 mL) was slowly added NaBH4 (120 mg, 3.12 mmol). The reaction was stirred at room temperature for 4 hours, before the addition of HCl solution (1 M, 50 mL). The stirring was kept at room temperature overnight. Then the solution was slowly concentrated in vacuo. Purification was accomplished by preparative HPLC to afford the title compound (108 mg, 32% yield) as a white lyophilizate. 1H NMR (400 MHz, DMSO-d6) δ ppm 9.23 (br. s., 1 H), 7.86 (br. s., 1 H), 7.79-7.68 (m, 2 H), 7.24 (s, 1 H), 7.18-7.13 (m, 1 H), 6.30 (d, J=8.6 Hz, 1 H), 4.98 (s, 2 H), 3.20 (d, J=1.6 Hz, 2 H), 3.17-3.06 (m, 5 H); ES-MS m/z=326 (M+H)+; HPLC: 99.39% (220 nm), 99.24% (MaxPlot).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012431B2
Source datasetuspto-grants-2015_04
ORD IDord-a0a0ba33b2d74a429b24e8dc83362b7b
Source noteuspto-grants-2015_04