Diisopropylcarbodiimide → HCID 59671565、化合物

温度

50 °C

Diisoproylcarbodiimide (0.028 mL, 0.178 mmol) was added to a solution of 2-(4-(tert-butoxycarbonyl)-2-((pyridin-3-yloxy)methyl)piperazin-1-yl)thiazole-4-carboxylic acid (68 mg, 0.162 mmol), methylamine hydrochloride (12 mg, 0.178 mmol), diisopropylethylamine (0.062 mL, 0.357 mmol), and N-hydroxybenzotriazole (24 mg, 0.178 mmol) in CH2Cl2 (2 mL). After stirring overnight, little reaction had taken place. TBTU (0.162 mmol) was added, and stirring was continued at rt. After 4 h, additional methylamine hydrochloride (20 mg, 0.296 mmol) was added, and the reaction was heated to 50° C. in a sealed vial overnight. Upon cooling to rt, the reaction mixture was quenched with 1 N NaOH (4 mL) and stirred for 1 h. The reaction mixture was diluted with EtOAc (20 mL) and was washed with 1 N NaOH (2×10 mL) and brine (10 mL), dried over Na2SO4, filtered, and concentrated under reduced pressure. The material was purified by column chromatography (40 to 90% EtOAc in hexanes gradient), yielding 35 mg (50%) of the title compound. LC-MS: RT=6.77 min, [M+H]+=434.7. Rf=0.10 in 100% EtOAc.

1. customlittle reaction
2. stirringstirring
3. customwas continued at rt
4. waitAfter 4 h
5. temperatureUpon cooling to rt
6. customthe reaction mixture was quenched with 1 N NaOH (4 mL)
7. stirringstirred for 1 h
8. additionThe reaction mixture was diluted with EtOAc (20 mL)
9. washwas washed with 1 N NaOH (2×10 mL) and brine (10 mL)
10. dry with materialdried over Na2SO4
11. filtrationfiltered
12. concentrationconcentrated under reduced pressure
13. customThe material was purified by column chromatography (40 to 90% EtOAc in hexanes gradient)

ORDレコード

ord-5e32e11d1454471e87e7231e15187b7e

出典データセット

uspto-grants-2014_09

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08822472B2