Hydrochloric Acid → (S)-1-((R)-2-Hydroxy-3,3-dimethyl-butyryl)-pyrrolidine-2-carboxylic acid 2-aminomethyl-5-chloro-benzylamide

온도

0 °C

1-((2R)-3,3-Dimethyl-2-hydroxybutanoyl)-N-(2-(tert-butyloxycarbonylaminomethyl)-5-chlorobenzyl)-L-prolinamide from the previous step (4.65 g, 9.65 mmol, HPLC RT=3.35 min) was dissolved in CH2Cl2 (15 mL) and cooled with stirring to 0° C. A solution of anhydrous HCl in ether (38 mL of a 1 Molar solution, 38 mmol) was added slowly. The resulting solution was stirred at 0° C. for 10 min, and then at ambient temperature for 20 h. The solid which had formed was collected by filtration and washed with several portions of ether. The solid was purified by preparative reverse-phase HPLC using an acetonitrile:water gradient containing 0.05% concentrated HCl. The product-containing fractions were combined and lyophilized to give the hydrochloride salt of the title compound as a white solid (HPLC RT=2.52 min, method A; LC-MS m/z=382; C, H, N combustion analysis, calculated for C19H28ClN3O3, 1.0HCl, 1.5H2O, calculated C, 51.24, H, 7.24, N, 9.43, found C, 51.32, H, 7.17, B, 9.33).

1. temperaturecooled
2. stirringThe resulting solution was stirred at 0° C. for 10 min
3. customThe solid which had formed
4. filtrationwas collected by filtration
5. washwashed with several portions of ether
6. customThe solid was purified by preparative reverse-phase
7. additionwater gradient containing 0.05% concentrated HCl

ORD 기록

ord-f949b0d351d94e6f863acd00f6d3537a

출처 데이터셋

uspto-grants-2003_02

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US06515011B2