Sodium borohydride → 6-chloro-N-2-thiazolyl-3-pyridinemethanamine

N-[(6-chloro-3-pyridinyl)methylene]-2-thiazolamine (i.e. the product of Step A) (0.55 g, 2.46 mmol) was added portionwise to a stirred excess of sodium borohydride (0.45 g, 11.8 mmol) in methanol (30 mL). Additional portions of sodium borohydride (2×1 equivalent) were added during the addition of the imine to maintain an exothermic reaction. After addition was complete, the reaction mixture was allowed to stir for 5 min at ambient temperature. The excess reducing agent was quenched by adding glacial acetic acid until gas evolution ceased. The clear reaction mixture was concentrated, and the resulting residue was partitioned between saturated aqueous sodium carbonate and ethyl acetate. The aqueous phase was extracted with ethyl acetate (3×30 mL), and the combined organic phases were washed with brine, dried (MgSO4) and concentrated to give the title compound as a tan powder (0.55 g).

1. temperatureto maintain
2. customan exothermic reaction
3. additionAfter addition
4. customwas quenched
5. additionby adding glacial acetic acid until gas evolution
6. concentrationThe clear reaction mixture was concentrated
7. customthe resulting residue was partitioned between saturated aqueous sodium carbonate and ethyl acetate
8. extractionThe aqueous phase was extracted with ethyl acetate (3×30 mL)
9. washthe combined organic phases were washed with brine
10. dry with materialdried (MgSO4)
11. concentrationconcentrated

ORD record

ord-de2fef16c8ce4c9c8988f896bf381ed6

Source dataset

uspto-grants-2013_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08552007B2