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HRID 1180748作成日:2026年10月25日

Phosgene → HCID 58979648、化合物

https://huagongshe.com/reaction/1180748

反応式

関与物質

役割名称HCID仕込み量
反応物PhosgeneHCID 6371—
反応物TriethylamineHCID 8471—
反応物(1-Benzylcyclohexyl)methanolHCID 58979707—
反応物N-((5S)-5-amino-6-hydroxy-7-oxo-7-{[(1R)-1-phenylethyl]amino}heptyl)-4-morpholinecarboxamide hydrochlorideHCID 69236903—
溶媒MethanolHCID 887—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 58979648HCID 5897964857%

反応手順

To a solution of 63 mg (0.31 mmol) of (1-benzylcyclohexyl)methanol in 1 mL of tetrahydrofuran was added 0.32 mL (0.62 mmol) of 1.93 M phosgene in toluene. The reaction was stirred at room temperature for 18 h, quenched with a stream of nitrogen gas for 5 min, and concentrated under reduced pressure. The resulting liquid was added to a solution of 133 mg (0.31 mmol) of N-((5S)-5-amino-6-hydroxy-7-oxo-7-{[(1R)-1-phenylethyl]amino}heptyl)-4-morpholinecarboxamide hydrochloride and 0.095 mL (0.68 mmol) of triethylamine in 2 mL of methanol. The reaction was stirred at room temperature for 24 h and concentrated under reduced pressure. The residue was purified by silica chromatography eluting with 6:4 acetone:hexanes to afford 110 mg (57%) of (1-benzylcyclohexyl)methyl(1S)-1-(1-hydroxy-2-oxo-2-{[(1R)-1-phenylethyl]amino}ethyl)-5-[(4-morpholinylcarbonyl)amino]pentylcarbamate. 1H NMR (400 MHz, DMSO-d6) δ 7.96 (m, 1H), 7.06-7.29 (m, 10H), 6.53 (d, J=9 Hz, 1H), 6.41 (m, 1H), 5.56-5.75 (m, 1H), 4.88 (qnt, J=7 Hz, 1H), 3.88 (m, 1H), 3.73 (m, 1H), 3.51 (m, 2H), 3.45 (t, J=4 Hz, 4H), 3.16 (t, J=4 Hz, 4H), 2.96 (m, 2H), 2.57 (s, 2H), 1.17-1.54 (m, 19H). ES-LCMS m/z 645 (M+Na).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07282512B2
出典データセットuspto-grants-2007_10
ORD IDord-c6590bde8d7a47498329f882ebb990ac
出典メモuspto-grants-2007_10