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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852375Generated: November 1, 2026

4-Methylmorpholine → Boc-Lys(Ac) aminocyanobenzothiazole

https://huagongshe.com/reaction/1852375

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantBoc-Lys(Ac)-OHHCID 7016049—
Reactant6-Amino-2-cyanobenzothiazoleHCID 14157112—
SolventTetrahydrofuranHCID 8028—
ProductBoc-Lys(Ac) aminocyanobenzothiazoleHCID 13173114393.4%

Reaction Steps

To a stirred solution of Boc-Lys-(Ac)—OH (20.5 g, 71 mmol) in dry THF (410 mL), N-methylmorpholine (7.8 mL, 71 mmol) was added under an atmosphere of N2. The reaction vessel was cooled to 4° C. for 20 minutes, at which time isobutylchloroformate (9.3 mL, 71 mmol) was added drop-wise. The reaction was allowed to stir in an ice bath for approximately 60 minutes, at which time 6-amino-2-cyanobenzothiazole (10 g, 57 mM) was added. The reaction was allowed to stir for approximately 30 minutes in the ice bath, removed, and the reaction mixture allowed to reach room temperature overnight. The reaction was then filtered through a Buchner funnel, and the filtrate concentrated to a solid foam. This solid foam was dissolved in dichloromethane (1 L) and washed 2× with NaHCO3 (sat. aq., 300 mL). The organic phase was dried over Na2SO4, filtered, and concentrated to provide a solid foam. This solid foam was then purified by silica gel chromatography with a gradient of heptane/ethyl acetate (EtOAc) (40% EtOAc to 100% EtOAc step gradient over 80 minutes) to provide 24.7 g of Boc-Lys(Ac)-aminocyanobenzothiazole as a foamy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962266B2
Source datasetuspto-grants-2015_02
ORD IDord-75236a855796412d8da82afe28beb6a7
Source noteuspto-grants-2015_02