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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32095Generated: October 29, 2026

Isobutyraldehyde → HCID 68930974, compound

https://huagongshe.com/reaction/32095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyraldehydeHCID 6561—
ReactantSodium borohydrideHCID 4311764—
Reactantn-[7-(2-Aminoethyl)-chroman-4-yl]-3-phenyl-3-(3-trifluoromethylbenzenesulfonylamino)-propionamideHCID 68929539—
CatalystAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 68930974HCID 68930974—

Reaction Steps

To a solution of N-[7-(2-aminoethyl)-chroman-4-yl]-3-phenyl-3-(3-trifluoromethylbenzenesulfonylamino)-propionamide (Example 208, 50 mg, 0.09 mmol) in dry CH2Cl2 (8 mL) was added isobutyraldehyde (83 L, 0.9 mmol) and HOAc (1 drop). The resulting mixture was stirred at RT under N2 After 3 h, MS showed the formation of imine; NaBH4 (17 mg, 0.45 mmol) was then added. The resulting mixture was stirred for 18 h. Quenched with minimum amount of sat. NaHCO3. The organic layer was isolated, dried over MgSO4 and evaporated in vacuo. The crude product was purified by chromatography on silica gel. Elution with CH2Cl2:MeOH mixture (97:3) gave final compound. MS m/z: 660.31 (M+H). Calc'd. for Calc'd. for C35H44F3N3O4S-659.82.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425631B2
Source datasetuspto-grants-2008_09
ORD IDord-b3232069b3924d23ae2ae225d2d9db74
Source noteuspto-grants-2008_09