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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174727Generated: November 2, 2026

3-Methylbutanal → HCID 11190455, compound

https://huagongshe.com/reaction/1174727

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethylbutanalHCID 11552—
ReactantSodium borohydrideHCID 4311764—
Reactant(4-Methanesulfonyl-phenyl)-[5-nitro-6-(piperidin-4-yloxy)-pyrimidin-4-yl]-amineHCID 11257886—
SolventMethanolHCID 887—
ProductHCID 11190455HCID 1119045536%

Reaction Steps

Compound A2 (0.15 mmol, 60 mg), and 3-methyl-butyraldehyde (0.15 mmol, 13 mg) were dissolved in methanol (2 mL) and stirred for 5 minutes at room temperature. Then, sodium borohydride (0.18 mmol, 6.3 mg) was added at 0° C. The reaction was complete immediately upon addition of sodium borohydride. The mixture was quenched with saturated ammonium chloride solution (1 mL) followed by an extraction with dichloromethane. Removal of organic solvent in vacuo and purification by HPLC provided Compound A8 as a yellow solid (25 mg, 36%). 1H NMR (400 MHz, CDCl3) δ (ppm): 10.17 (s, 1H), 8.35 (s, 1H), 7.90 (d, 2H), 7.80 (d, 2H), 5.72 (s broad, 1H), 3.65 (m, 2H), 3.11 (m, 2H), 2.96 (m, 5H), 2.40 (m, 2H), 2.15 (m, 2H), 1.60 (m, 3H), 0.85 (d, 6H). LCMS (ESI), m/z 464.4 (M+H+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838525B2
Source datasetuspto-grants-2010_11
ORD IDord-1ac15d343190401791ce0920d919636a
Source noteuspto-grants-2010_11