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HRID 710124作成日:2026年10月25日

1-(4-bromophenyl)-1H-tetrazole → Tert-butyl 4-{5-[4-(1H-tetrazol-1-yl)phenyl]benzo[d]oxazol-2-yl}piperidine-1-carboxylate

https://huagongshe.com/reaction/710124

反応式

関与物質

役割名称HCID仕込み量
反応物1-(4-bromophenyl)-1H-tetrazoleHCID 560805—
反応物Tert-butyl 4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]oxazol-2-yl)piperidine-1-carboxylateHCID 71090269—
生成物Tert-butyl 4-{5-[4-(1H-tetrazol-1-yl)phenyl]benzo[d]oxazol-2-yl}piperidine-1-carboxylateHCID 7111419740.7%

反応手順

Following the General Procedure-1, the titled compound (80 mg) was prepared from Intermediate 8 (200 mg, 0.47 mmol) and 1-(4-bromophenyl)-1H-tetrazole (100 mg, 0.44 mmol) as a brown solid. M.P.: 207-211° C. 1H-NMR (δ ppm, CDCl3, 400 MHz): 9.02 (s, 1H), 7.91 (d, J 1.2, 1H), 7.82-7.79 (m, 4H), 7.62-7.55 (m, 2H), 4.16 (d, J 10.6, 2H), 3.21-3.12 (m, 1H), 3.00 (t, J 12.3, 2H), 2.20-2.14 (m, 2H), 2.00-1.88 (m, 2H), 1.48 (s, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181214B2
出典データセットuspto-grants-2015_11
ORD IDord-4e45b60788ae4abf87560b8579386d79
出典メモuspto-grants-2015_11