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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515508Generated: October 29, 2026

Hydrochloric Acid → 5-Chloro-2-(5-methyl-1,4-diazepan-1-yl)-1,3-benzoxazole

https://huagongshe.com/reaction/515508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantSodium AcetateHCID 517045—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-[(2-Aminoethyl)(5-chloro-2-benzoxazolyl)amino]-2-butanoneHCID 53260161—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product5-Chloro-2-(5-methyl-1,4-diazepan-1-yl)-1,3-benzoxazoleHCID 53260162—

Reaction Conditions

Temperature15 °C

Reaction Steps

Bis-MSA adduct 12 (17.19 kg, 36.27 mol), sodium acetate (2.97 kg, 36.3 mol) and DCM (152 kg, 115 L) were charged to a vessel. The resulting slurry was cooled to 15° C. and acetic acid (26.8 kg, this was the amount required for dissolution of the salt) was added maintaining an internal temperature below 20° C. The batch was cooled to 15° C. and Na(OAc)3BH (9.25 kg, 43.6 mol) was charged via a glove bag over 30 min maintaining an internal temperature below 20° C. The resulting solution was aged for 30 min at 20° C., HPLC analysis showed the reaction to be complete. The batch was then cooled to 10° C., 2N HCl (38.80 kg) was added and the resulting solution was aged for 30 min at 10° C. The mixture was then adjusted to pH 9 using 5 N NaOH maintaining an internal temperature below 20° C. Once at pH 9 the layers were allowed to separate and the organic lower layer was ran off into a clean drum. DCM (76.2 kg, 57.5 L) was then added to the aqueous phase, the layers were mixed, allowed to separate, then the lower layer was combined with the previous organics (this step was repeated but HPLC of the third DCM layer showed that this was unnecessary as it only contained 12.5 g of rac-11 by assay). The combined DCM fractions were then charged to a 160 liter vessel and distilled to approximately 20 L (˜1 volume of DCM). THF (44 kg) was charged to the vessel and the resulting stream was discharged into a clean drum and stored in the cold room prior to the next step in the reaction sequence. The final solution was found to contain 9.4 kg of rac-14. This stream was sufficiently pure to be used directly in the subsequent resolution.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108959B2
Source datasetuspto-grants-2015_08
ORD IDord-4e484496e6e8459289e4fd56d81d3b4e
Source noteuspto-grants-2015_08