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HRID 23733作成日:2026年10月24日

Benzyl isocyanate → (4-{[Benzyl({[3,5-bis(trifluoromethyl)benzoyl]amino}sulfonyl)amino]methyl}cyclohexyl)methyl 2-phenylethylcarbamate

https://huagongshe.com/ja/reaction/23733

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Phenethyl isocyanateHCID 160602—
反応物(4-{[Benzyl({[3,5-bis(trifluoromethyl)benzoyl]amino}sulfonyl)amino]methyl}cyclohexyl)methyl benzylcarbamateHCID 22574464—
生成物(4-{[Benzyl({[3,5-bis(trifluoromethyl)benzoyl]amino}sulfonyl)amino]methyl}cyclohexyl)methyl 2-phenylethylcarbamateHCID 22574475—

反応手順

Following procedure to make (9), phenethyl isocyanate was substituted for benzyl isocyanate to give the title compound after purification. 1H NMR (500 MHz, DMSO-d6): δ 12.43 (s, 1H), 8.45 (s, 2H), 8.10 (s, 1H), 7.37 (d, 2H), 7.27 (t, 3H), 7.16 (m, 3H), 7.07 (t, 2H), 4.34 (s, 2H), 3.61 (d, 2H), 3.14 (m, 2H), 3.30 (water), 2.88 (d, 2H), 2.66 (t, 2H), 2.48 (DMSO), 1.62 (m, 2H), 1.52 (m, 2H), 1.32 (m, 1H), 1.26 (m, 1H), 0.63 (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-5bbeaa3f00ff4371874d44bdbf2cdc73
出典メモuspto-grants-2005_02