Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625809Generated: October 29, 2026

Hydrochloric Acid → HCID 46893388, compound

https://huagongshe.com/reaction/625809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantMeOH tetrahydrofuranHCID 21899815—
ReactantHCID 46892241HCID 46892241—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 46893388HCID 4689338833.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To (3-fluorophenyl)(4-(5-methyl-1H-pyrazol-3-ylamino)quinazolin-2-yl)methanone from Example 1 (0.15 g, 0.43 mmol) in 1:1 THF/MeOH (4 mL) at 0° C. was added sodium borohydride (0.02 g, 0.58 mmol) and the mixture was stirred at 0° C. for 30 min. To the mixture were added 6 N HCl and DMSO (3 mL), and the mixture was purified by preparative HPLC (Varian diphenyl reverse phase column eluting with gradient of solvent B=0.05% HOAC/MeOH and solvent A=0.05% HOAc/H2O) to afford (3-fluorophenyl)(4-(5-methyl-1H-pyrazol-3-ylamino)quinazolin-2-yl)methanol (50 mg, 32%). 1H NMR (300 MHz, DMSO-d6) δ 2.26 (s, 3H) 5.7 (s, 1H) 5.93 (s, 1H) 6.44 (s, 1H) 7.07 (m, 1H) 7.34-7.39 (m, 3H) 7.54 (m, 1H) 7.81 (s, 2H) 8.59 (d, 1H) 10.42 (s, 1H) 12.15 (s, 1H); LC-MS (ESI) m/z 350 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09308207B2
Source datasetuspto-grants-2016_04
ORD IDord-501a350044294e159b556acec39479dc
Source noteuspto-grants-2016_04