Hydrochloric Acid → HCID 86730046, compound

Methyl 1-amino-3-((R)-6-hexyl-5,6,7,8-tetrahydronaphthalen-2-yl)cyclopentanecarboxylate (I-8F, 5.7 g, 16 mmol) was dissolved in EtOH (60 mL) and methylene chloride (15 mL). Sodium borohydride (2.5 g, 67 mmol) was added. The mixture was stirred at room temperature overnight. Hydrochloric acid (6 N aqueous, 40 mL) was added slowly at 0° C. to make pH approximately 1. After the mixture was stirred at room temperature for 60 min, sodium hydroxide (10 g in 20 mL of water) was added to make pH approximately 12. The mixture was stirred at room temperature for 40 min before being concentrated to remove organic solvents. The aqueous residue was diluted with water (20 mL) and extracted with EtOAc (100 mL, 2×50 mL). The combined ethyl acetate extracts were dried over anhydrous sodium sulfate, decolored by charcoal, filtered through CELITE® pad, and concentrated under reduced pressure to give (1-amino-3-((R)-6-hexyl-5,6,7,8-tetrahydronaphthalen-2-yl)cyclopentyl)methanol (5.0 g, 15 mmol) as a white solid.

1. stirringAfter the mixture was stirred at room temperature for 60 min
2. stirringThe mixture was stirred at room temperature for 40 min
3. concentrationbefore being concentrated
4. customto remove organic solvents
5. additionThe aqueous residue was diluted with water (20 mL)
6. extractionextracted with EtOAc (100 mL, 2×50 mL)
7. dry with materialThe combined ethyl acetate extracts were dried over anhydrous sodium sulfate
8. filtrationfiltered through CELITE® pad
9. concentrationconcentrated under reduced pressure

ORD record

ord-f62255ad98134eeba33a7eee213fd55b

Source dataset

uspto-grants-2016_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09359286B2