Triethylamine → 1-(1H-Imidazol-5-ylmethyl)-2-thioxo-1,2,3,5-tetrahydro-pyrrolo[3,2-d]pyrimidin-4-one

3-Amino-1H-pyrrole-2-carboxylic acid ethyl ester hydrochloride (0.10 g, 0.52 mmol) was dissolved in methanol (4 mL) and 4-formylimidazole (0.060 g, 0.63 mmol), NaCNBH3 (0.033 g, 0.52 mmol) and Et3N (0.073 g, 0.52 mmol) were added. The resulting mixture was stirred at r.t. overnight. The solvent was removed in vacuo and the residue was dissolved in CH2Cl2 (3 mL) and methanol (1 mL). Benzoyl isothiocyanate (0.078 mL, 0.58 mmol) was added and after stirring at r.t. for 30 minutes the mixture was concentrated in vacuo. The residue was dissolved in ammonia (7N in methanol, 3 mL) and heated at 80° C. for 1 h. The precipitated product was filtered and washed with methanol, followed by diethyl ether. The crude product was purified by preparative HPLC, obtaining 0.017 g (13%) of the title compound as a solid. OC 710/07

1. customThe solvent was removed in vacuo
2. dissolutionthe residue was dissolved in CH2Cl2 (3 mL)
3. stirringafter stirring at r.t. for 30 minutes the mixture
4. concentrationwas concentrated in vacuo
5. dissolutionThe residue was dissolved in ammonia (7N in methanol, 3 mL)
6. temperatureheated at 80° C. for 1 h
7. filtrationThe precipitated product was filtered
8. washwashed with methanol
9. customThe crude product was purified by preparative HPLC

ORDレコード

ord-8df471470c194193998dd4ad29a66638

出典データセット

uspto-grants-2014_10

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08859568B2