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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504710Generated: October 26, 2026

Acetaldehyde → HCID 59135843, compound

https://huagongshe.com/reaction/504710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantWaterHCID 962—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-methyl-N-[2-(1-thia-3,8-diazaspiro[4.5]dec-2-en-2-yl)-1H-indol-7-yl]thiophene-2-sulfonamideHCID 59135835—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59135843HCID 5913584380%

Reaction Steps

To a solution of N-methyl-N-[2-(1-thia-3,8-diazaspiro[4.5]dec-2-en-2-yl)-1H-indol-7-yl]thiophene-2-sulfonamide (100 mg) and acetaldehyde (90%) (100 μL) in tetrahydrofuran (3 ml) was added sodium triacetoxyborohydride (125 mg), and the mixture was stirred at room temperature for 30 min. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4), and concentrated. The obtained residue was subjected to silica gel column chromatography to give the title compound (83 mg, yield 80%) as colorless crystals from a fraction eluted with ethyl acetate. melting point 215° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777047B2
Source datasetuspto-grants-2010_08
ORD IDord-ce503f1f15534102874521bf95e8dc2c
Source noteuspto-grants-2010_08