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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785439Generated: October 29, 2026

Acetone → HCID 11306778, compound

https://huagongshe.com/reaction/1785439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantDichloromethaneHCID 6344—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 57593142HCID 57593142—
SolventMethanolHCID 887—
ProductHCID 11306778HCID 11306778—

Reaction Steps

To a solution of 7-(2-Amino-ethyl)-9-(2-phenethylamino-pyrimidin-4-yl)-2-phenyl-6,7,8,9-tetrahydro-pyrimido[1,2-a]pyrimidin-4-one (70 mg, 0.15 mmol), acetone (0.02 mL), dichloromethane (0.5 mL) and methanol (0.5 mL) was added sodium triacetoxyborohydride (38 mg, 0.18 mmol) Reaction stirred for 2 h at room temperature. Solvents removed under vacuum. Residue partitioned between dichloromethane and 5% sodium bicarbonate. Organics purified on silica to afford a white solid. M+1=510. 1NMR (CDCl3) d (6H, 1.17 ppm), m (2H, 1.68 ppm), m (1H, 2.32 ppm), m (3H, 2.78 ppm), t (2H, 2.94 ppm), m (1H, 3.55 ppm), dd (2H, 3.70 ppm), d (1H, 4.40 ppm), dd (1H, 4.53 ppm), m (1H, 5.10 ppm), s (1H, 6.60 ppm), m (3H, 7.24 ppm), m (2H, 7.32 ppm), m (3H, 7.44 ppm), m (2H, 7.90 ppm) d (1H, 8.18 ppm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504403B2
Source datasetuspto-grants-2009_03
ORD IDord-13259bf123d54673ac4b4e67de5cd963
Source noteuspto-grants-2009_03