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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326707Generated: October 30, 2026

Sodium borohydride → HCID 19735302, compound

https://huagongshe.com/reaction/326707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 53682521HCID 53682521—
SolventMethanolHCID 887—
ProductHCID 19735302HCID 1973530278.9%

Reaction Steps

53 mg of rac-p-[[5-(o-methoxybenzyl)-6-[2-[(tetrahydro-2H-pyran-2-yl]oxy]ethoxy]-4-pyrimidinyl]sulfamoyl]benzalde-hyde were dissolved in 3 ml of methyl alcohol and treated with 37 mg of sodium borohydride at room temperature. After stirring at room temperature for 1 hour, the methanol was evaporated under reduced pressure. The residue was dissolved in ethyl acetate, washed with water and NaCl solution (saturated), dried and distilled under reduced pressure. There were obtained 42 mg of rac-α-hydroxy-N-[5-(o-methoxybenzyl)-6-[2-[(tetra-hydro-2H-pyran-2-yl)oxy]ethoxy]-4-pyrimidinyl]-p-toluene-sulfonamide as a colorless oil. MS: 529 (M); 445 (tetrahydro-2H-pyran-2-yl); 434 (--OCH3 +SO2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05270313
Source datasetuspto-grants-1993_12
ORD IDord-821affe0864647749aa63b8ef07cc106
Source noteuspto-grants-1993_12