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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900664Generated: October 30, 2026

Sodium triacetoxyborohydride → HCID 21978572, compound

https://huagongshe.com/reaction/900664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(3-Oxo-[1,4]oxazepan-4-yl)-butyraldehydeHCID 21978718—
ReactantHCID 69223720HCID 69223720—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 21978572HCID 21978572—

Reaction Steps

A mixture of ethyl-{(S)-1-methyl-2-[4-(thiazole-2-sulfonyl)phenyl]ethyl}-amine (0.326 g, 1.02 mmole), 4-(3-oxo-[1,4]oxazepan-4-yl)-butyraldehyde (0.22 g, 1.2 mmole), and sodium triacetoxyborohydride (0.3 g, 1.4 mmole) in 1,2-dichloroethane (10 mL) was stirred at room temperature for 15 hours. The solvent was removed under reduced pressure and the residue was partitioned between 5% hydrochloric acid and diethyl ether. The aqueous phase was brought to pH 12 with 25% sodium hydroxide and the mixture was extracted with dichloromethane. The organic phase was dried (magnesium sulfate) and concentrated to give 4-(4-{ethyl-[2-(4-thiazole-2-sulfonylphenyl)-1-methylethyl]amino}butyl)-[1,4]oxazepan-3-one, 145, as an oil. Anal.: Calcd. for C23H34ClN3O4S2.1H2O: C, 51.72; H, 6.79; N, 7.87%. Found C, 51.71; H, 6.49 N, 7.82%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361648B2
Source datasetuspto-grants-2008_04
ORD IDord-ed5cc99a0fd040aca429ab66856ddb48
Source noteuspto-grants-2008_04