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HRID 23734作成日:2026年10月24日

Benzyl isocyanate → (4-{[Benzyl({[3,5-bis(trifluoromethyl)benzoyl]amino} sulfonyl)amino]methyl}cyclohexyl)methyl 3-methoxyphenylcarbamate

https://huagongshe.com/ja/reaction/23734

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl isocyanateHCID 76639—
反応物DiisopropylethylamineHCID 81531—
反応物3-Methoxyphenyl isocyanateHCID 87843—
反応物(4-{[Benzyl({[3,5-bis(trifluoromethyl)benzoyl]amino}sulfonyl)amino]methyl}cyclohexyl)methyl benzylcarbamateHCID 22574464—
溶媒TriethylamineHCID 8471—
生成物(4-{[Benzyl({[3,5-bis(trifluoromethyl)benzoyl]amino} sulfonyl)amino]methyl}cyclohexyl)methyl 3-methoxyphenylcarbamateHCID 22574485—

反応手順

Following procedure to make (9), 3-methoxyphenyl isocyanate was substituted for benzyl isocyanate and diisopropylethylamine substituted for triethylamine to give the title compound after purification. 1H NMR (500 MHz, DMSO-d6): δ 9.50 (s, 1H), 8.45 (s, 2H), 8.10 (s, 1H), 7.38 (d, 2H), 7.24 (t, 2H), 7.14 (m, 3H), 6.96 (d, 1H), 6.52 (d, 1H), 4.35 (s, 2H), 3.75 (d, 2H), 3.68 (s, 3H), 3.30 (water), 2.89 (d, 2H), 2.48 (DMSO), 1.63 (m, 4H), 1.42 (m, 1H), 1.29 (m, 1H), 0.66 (m, 4H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06852738B2
出典データセットuspto-grants-2005_02
ORD IDord-3754d13e72ce47f49728e435d6baaf46
出典メモuspto-grants-2005_02