Water → HCID 86681009, compound

Temperature

0 °C

To a solution of 2-(methylthio)benzo[d]thiazole-6-carbonitrile (10.0 g, 48.5 mmol) from Step 3 of this Example in THF (150 mL) was added lithium aluminum hydride solution (2.0 M in THF, 50.9 mL, 101.9 mmol) slowly at −78° C. The reaction mixture was slowly warmed to 0° C. and stirred at 0° C. for 3 h treated with 4 mL of water, 4 mL of 10% aq NaOH and 12 mL of water. The resulting reaction mixture was stirred at rt for 1 h before it was filtered through a Celite pad and the precipitates were washed with 100 of mL EtOAc. The combined filtrates were concentrated under reduced pressure. The crude product was purified on a silica gel column using a mixture of MeOH—CH2Cl2 (1:2, v/v) as eluent to give (2-(methylthio)benzo[d]thiazol-6-yl)methanamine as an yellow oil (3.5 g, 34%). 1H NMR (300 MHz, CDCl3) δ 7.82 (d, J=8.3 Hz, 1H), 7.73 (s, 1H), 7.35 (dd, J=1.4, 8.4 Hz, 1H), 3.97 (s, 2H), 2.79 (s, 3H), 1.55 (s, 2H). LCMS (ESI) m/z 211 (M+H)+.

1. customslowly at −78° C
2. customThe resulting reaction mixture
3. stirringwas stirred at rt for 1 h before it
4. filtrationwas filtered through a Celite pad
5. washthe precipitates were washed with 100 of mL EtOAc
6. concentrationThe combined filtrates were concentrated under reduced pressure
7. customThe crude product was purified on a silica gel column
8. additiona mixture of MeOH—CH2Cl2 (1:2

ORD record

ord-af75f8dd413a41a1b0f9a7ee1278a3c1

Source dataset

uspto-grants-2015_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08952058B2