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

HRID 23734

Reaktionsgleichung

Reaktionsgleichung von HRID 23734
C(NC(=O)O[CH2:11][CH:12]1[CH2:17][CH2:16][CH:15]([CH2:18][N:19]([CH2:40][C:41]2[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=2)[S:20]([NH:23][C:24](=[O:39])[C:25]2[CH:30]=[C:29]([C:31]([F:34])([F:33])[F:32])[CH:28]=[C:27]([C:35]([F:38])([F:37])[F:36])[CH:26]=2)(=[O:22])=[O:21])[CH2:14][CH2:13]1)C1C=CC=CC=1.[CH3:48][O:49][C:50]1[CH:51]=[C:52]([N:56]=[C:57]=[O:58])[CH:53]=[CH:54][CH:55]=1.C(N=C=[O:68])C1C=CC=CC=1.C(N(C(C)C)CC)(C)C>C(N(CC)CC)C>[CH3:48][O:49][C:50]1[CH:51]=[C:52]([NH:56][C:57](=[O:68])[O:58][CH2:11][CH:12]2[CH2:17][CH2:16][CH:15]([CH2:18][N:19]([CH2:40][C:41]3[CH:42]=[CH:43][CH:44]=[CH:45][CH:46]=3)[S:20]([NH:23][C:24](=[O:39])[C:25]3[CH:30]=[C:29]([C:31]([F:32])([F:33])[F:34])[CH:28]=[C:27]([C:35]([F:36])([F:37])[F:38])[CH:26]=3)(=[O:21])=[O:22])[CH2:14][CH2:13]2)[CH:53]=[CH:54][CH:55]=1

Komponenten

6

Versuchsvorschrift

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).

Quellen und Nachweise

ORD-Eintrag
ord-3754d13e72ce47f49728e435d6baaf46
Quelldatensatz
uspto-grants-2005_02
Patentnummer
US06852738B2

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