Ethanol → 2-(2-benzyloxyphenyl)-N-methylacetamide

온도

0 °C

(2R)-2-(N-((2E)-5-Amino-5-methylhex-2-enoyl)-N-methylamino)-N-(2-(2-(3-hydroxypropoxy)phenyl)ethyl)-N-methyl-3-(2-naphthyl)propionamide ##STR173## 2-(2-Benzyloxyphenyl)-N-methylacetamide ##STR174## 2-(2-Benzyloxyphenyl)acetic acid (15.0 g, 62 mmol) was dissolved in dichloromethane (270 ml) and N,N-dimethylformamide (70 ml). 1-Hydroxybenzotriazole (8.37 g, 62 mmol) was added. The solution was cooled to 0° C. N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (11.89 g, 62 mmol) was added. The reaction mixture was stirred for 20 min. A 8.0M solution of methylamine in ethanol (38.8 ml, 310 mmol) was added. The solution was stirred for 16 h, while it was warming up to room temperature. It was diluted with ethyl acetate (500 ml) and washed with a 10% aqueous solution of sodium hydrogen sulfate solution (500 ml). The aqueous phase was extracted with ethyl acetate (2×300 ml). The combined organic layers were washed with a saturated aqueous solution of sodium hydrogen carbonate (400 ml) and dried over magnesium sulfate. The solvent was removed in vacuo. The remaining crystals were washed with a mixture of ethyl acetate/heptane 1:4 (100 ml). They were dried in vacuo. They were dissolved in ethyl acetate. The solution was washed with a saturated aqueous solution of sodium hydrogen carbonate (2×500 ml) and dried over magnesium sulfate. The solvent was removed in vacuo to give 10.24 g of 2-(2-benzyloxyphenyl)-N-methylacetamide.

1. stirringThe solution was stirred for 16 h, while it
2. temperaturewas warming up to room temperature
3. washwashed with a 10% aqueous solution of sodium hydrogen sulfate solution (500 ml)
4. extractionThe aqueous phase was extracted with ethyl acetate (2×300 ml)
5. washThe combined organic layers were washed with a saturated aqueous solution of sodium hydrogen carbonate (400 ml)
6. dry with materialdried over magnesium sulfate
7. customThe solvent was removed in vacuo
8. washThe remaining crystals were washed with a mixture of ethyl acetate/heptane 1:4 (100 ml)
9. customThey were dried in vacuo
10. dissolutionThey were dissolved in ethyl acetate
11. washThe solution was washed with a saturated aqueous solution of sodium hydrogen carbonate (2×500 ml)
12. dry with materialdried over magnesium sulfate
13. customThe solvent was removed in vacuo

ORD 기록

ord-2976ef68c5644af2b7f0fd7d4f4cb9aa

출처 데이터셋

uspto-grants-1999_07

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US05922770