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HRID 80701作成日:2026年10月24日

Formic Acid → HCID 178507110、化合物

https://huagongshe.com/ja/reaction/80701

反応式

関与物質

役割名称HCID仕込み量
反応物Formic AcidHCID 284—
反応物benzyl(3-(benzyloxy)-2-(4-chloro-5-(4-fluorobenzyl)-1H-imidazol-2-yl)-4-oxo-6,7,8,9-tetrahydro-7,10-ethanopyrimido[1,2-a]azepin-10(4H)-yl)carbamateHCID 117616853—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物HCID 178507110HCID 17850711083%

反応条件

温度40 °C

反応手順

To a solution of benzyl(3-(benzyloxy)-2-(4-chloro-5-(4-fluorobenzyl)-1H-imidazol-2-yl)-4-oxo-6,7,8,9-tetrahydro-7,10-ethanopyrimido[1,2-a]azepin-10(4H)-yl)carbamate, Intermediate 6 (60 mg, 0.092 mmol) in MeOH (3 mL) was added formic acid (0.100 mL, 2.65 mmol) followed by 10% Pd/C (98 mg, 0.092 mmol) and the mixture stirred at 40° C. for 3 h. After cooling to room temperature, the mixture was filtered through a pad of celite and concentrated. The mixture was then treated with sat. NaHCO3, extracted with dichloromethnae (×4), dried (Na2SO4), filtered and concentrated to afford the title compound (30 mg, 83% yield) as a light purple solid. 1H NMR (500 MHz, DMSO-d6) δ ppm 1.53-1.60 (m, 2H), 1.73-1.81 (m, 6H), 2.37 (br. s., 1H), 2.51-2.54 (m, 2H), 3.93-3.99 (m, 2H), 4.01 (d, J=3.66 Hz, 2H), 7.10-7.17 (m, 3H), 7.30 (dd, J=8.24, 5.80 Hz, 2H). LCMS (M+H)=396.13.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846659B2
出典データセットuspto-grants-2014_09
ORD IDord-4dae1b8a5d654082b51557eb41856b84
出典メモuspto-grants-2014_09