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HRID 1013207作成日:2026年10月26日

Phenethyl bromide → [3-(1,1-Dioxo-2-phenethyl-2,3-dihydro-1h-1lambda6-benzo[d]isothiazol-3-yl)-5-methoxy-indol-1-yl]-acetic acid

https://huagongshe.com/reaction/1013207

反応式

関与物質

役割名称HCID仕込み量
反応物Phenethyl bromideHCID 7666—
反応物[3-(1,1-Dioxo-2,3-dihydro-1h-1lambda6-benzo[d]isothiazol-3-yl)-5-methoxy-indol-1-yl]-acetic acid tert-butyl esterHCID 67316901—
生成物[3-(1,1-Dioxo-2-phenethyl-2,3-dihydro-1h-1lambda6-benzo[d]isothiazol-3-yl)-5-methoxy-indol-1-yl]-acetic acidHCID 59753843—

反応手順

The title compound was prepared by the method described for example 14 using the product from example 4, step c) and 2-bromoethylbenzene. 1H NMR (DMSO-d6) 13.03 (bs, 1H), 7.98 (d, J=8.7 Hz, 1H), 7.65-7.60 (m, 2H), 7.50 (s, 1H), 7.29 (d, J=9.0 Hz, 1H), 7.25-7.13 (m, 4H), 7.09 (d, J=8.1 Hz, 2H), 6.74 (dd, J=2.4, 9.0 Hz, 1H), 6.54 (d, J=2.4 Hz, 1H), 5.95 (s, 1H), 5.00 (s, 2H), 3.51 (s, 3H), 3.42 (ddd, J=6.3, 10.2, 15.9 Hz, 1H), 3.14 (ddd, J=5.7, 9.9, 15.0 Hz, 1H), 3.00-2.70 (m, 2H); MS: ESI (negative): 475 (M−H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07981912B2
出典データセットuspto-grants-2011_07
ORD IDord-f9b3487ef5e34ca3938e4630fb3e9761
出典メモuspto-grants-2011_07