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HRID 897045作成日:2026年10月25日

Mecloqualone → 3-(2-Chloro-phenyl)-2-(2-dimethylamino-vinyl)-3,4-dihydro-quinazolin-4-one

https://huagongshe.com/reaction/897045

反応式

関与物質

役割名称HCID仕込み量
反応物MecloqualoneHCID 9567—
反応物Dimethylformamide dimethyl acetalHCID 78373—
溶媒DimethylformamideHCID 6228—
生成物3-(2-Chloro-phenyl)-2-(2-dimethylamino-vinyl)-3,4-dihydro-quinazolin-4-oneHCID 5368976962.4%

反応条件

温度140 °C

反応手順

A mixture of 3-(2-chloro-phenyl)-2-methyl-3,4-dihydro-quinazolin-4-one (1.0 g, 3.69 mmol) and dimethylformamide dimethyl acetal (0.64 mL, 4.8 mmol) in dimethylformamide (4 mL) was heated to 140° C. for 24 hours. Additional dimethylformamide dimethyl acetal (0.32 mL, 2.4 mmol) was added and heating was continued for an additional 24 hours. The reaction was cooled to ambient temperature and concentrated at reduced pressure (60° C. bath temperature). The dark residue was triturated with methanol and the pale orange solid which formed was collected and dried to give 0.75 g (62%) of 3-(2-chloro-phenyl)-2-(2-dimethylamino-vinyl)-3,4-dihydro-quinazolin-4-one which had: mp 228-230° C.; 1H 1H NMR δ 8.19 (d, J=8 Hz, 1 H), 7.91 (d, J=12.3 Hz, 1 H), 7.71-7.18 (m, 7 H), 4.10 (d, J=12.3 Hz, 1 H), 2.81 (br s, 6 H). Analysis calculated for C18H16ClN3O: C, 66.36; H, 4.95; N, 12.90. Found: C, 66.20; H, 5.03; N, 12.79.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06921764B2
出典データセットuspto-grants-2005_07
ORD IDord-9ec17971598e4b4e8f829fb8df34cf1d
出典メモuspto-grants-2005_07