Sodium Hydroxide → HCID 22226742, compound

Temperature

-7.5 °C

To a solution of 3-amino-6-(methylsulfonyl)pyridine (3.72 g, 21.6 mmol) in concentrated hydrochloric acid (30 mL), sodium nitrite (1.78 g, 25.7 mmol) in water (20 mL) was added dropwise at −10 to −15° C. and the mixture was stirred for 2 hours at −10 to −5° C. (note: the reaction was monitored by thin layer chromatography to make sure all the starting material was consumed). Tin(II) chloride dihydrate (20 g, 88.6 mmol) in concentrated hydrochloric acid (30 mL) was added dropwise at −5° C. The mixture was stirred 1 hour at −5° C. and then left overnight. The mixture was basified with aqueous sodium hydroxide (pH=9) with ice cooling and tetrahydrofuran (200 mL) was added and stirred for 30 minutes. The mixture was filtered through Celite® and the filtrate was extracted with tetrahydrofuran (200 mL×3). The organic extraction was combined and dried over magnesium sulfate and concentrated under reduced pressure to provide the title compound (3.2g, 78.8%).

1. customwas consumed)
2. stirringThe mixture was stirred 1 hour at −5° C.
3. waitleft overnight
4. additionwas added
5. stirringstirred for 30 minutes
6. filtrationThe mixture was filtered through Celite®
7. extractionthe filtrate was extracted with tetrahydrofuran (200 mL×3)
8. extractionThe organic extraction
9. dry with materialdried over magnesium sulfate
10. concentrationconcentrated under reduced pressure

ORD record

ord-6f95a5839f3740639f640f56e78c33f6

Source dataset

uspto-grants-2003_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06531492B1