반응 #1100107

ord-abbd24cdbabb449baab03d1664403dee

반응 조건

상세 조건
See reaction.notes.procedure_details.

실험 절차

The title compound was prepared according to the same protocol as that described for example 1, steps 1.a to 1.c, starting from 4-ethoxy-benzothiazole (5 mmol), [trans-4-(methoxy-methyl-carbamoyl)-cyclohexyl]-carbamic acid tert-butyl ester (2.5 mmol) and 3-oxo-3,4-dihydro-2H-benzo[1,4]oxazine-6-carbaldehyde (0.3 mmol). A yellowish solid (9 mg) was obtained.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07981886B2uspto-grants-2011_07