Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336218Generated: October 30, 2026

Sodium cyanoborohydride → (S)-1-(Tetrahydro-pyran-4-ylmethyl)-azepane-2-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amide

https://huagongshe.com/reaction/336218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantTetrahydro-2H-pyran-4-carboxaldehydeHCID 9964078—
Reactant(S)-Perhydro-azepine-2-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amide hydrochlorideHCID 86660403—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(S)-1-(Tetrahydro-pyran-4-ylmethyl)-azepane-2-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amideHCID 58563913—

Reaction Steps

Sodium cyanoborohydride (0.19 g, 3.02 mmol) and tetrahydro-pyran-4-carbaldehyde (0.26 g, 2.26 mmol) is added to a solution of (S)-perhydro-azepine-2-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amide hydrochloride (prepared according to Method T, step 6) (0.4 g, 1.51 mmol) in DMF (5.0 mL). After stirring for four hours, the reaction mixture is diluted with EtOAc and washed twice with water. The organic phase is dried over anhydrous Na2SO4 and after removal of the solvent under reduced pressure, the crude is purified by prep TLC to afford the title compound; m/z 364 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889670B2
Source datasetuspto-grants-2014_11
ORD IDord-e9cb4a17530d4635900ad0729b303dbb
Source noteuspto-grants-2014_11