HCID 70007818, compound → HCID 18619663, compound

HRID 1862781Notes

Reaction equation

HRID 1862781 reaction equation
[Si]([O:18][C:19]1[CH:60]=[CH:59][C:22]([O:23][CH2:24][C@@H:25]([OH:58])[CH2:26][NH:27][CH2:28][CH2:29][C:30]2[CH:35]=[CH:34][C:33]([N:36]3[C:40]4=[N:41][CH:42]=[CH:43][CH:44]=[C:39]4[N:38]=[C:37]3[C:45]3[CH:50]=[CH:49][C:48]([N:51]4[CH:55]=[CH:54][C:53]([CH3:56])=[N:52]4)=[CH:47][C:46]=3[Cl:57])=[CH:32][CH:31]=2)=[CH:21][CH:20]=1)(C(C)(C)C)(C1C=CC=CC=1)C1C=CC=CC=1>C(Cl)(Cl)Cl.CO>[Cl:57][C:46]1[CH:47]=[C:48]([N:51]2[CH:55]=[CH:54][C:53]([CH3:56])=[N:52]2)[CH:49]=[CH:50][C:45]=1[C:37]1[N:36]([C:33]2[CH:34]=[CH:35][C:30]([CH2:29][CH2:28][NH:27][CH2:26][CH:25]([OH:58])[CH2:24][O:23][C:22]3[CH:21]=[CH:20][C:19]([OH:18])=[CH:60][CH:59]=3)=[CH:31][CH:32]=2)[C:40]2=[N:41][CH:42]=[CH:43][CH:44]=[C:39]2[N:38]=1

Participants

3

Procedure

(2S)-1-(4-{[tert-Butyl(diphenyl)silyl]oxy}phenoxy)-3-[(4-{2-[2-chloro-4-(3-methyl-1H-pyrazol-1-yl)phenyl]-3H-imidazo[4,5-b]pyridin-3-yl}phenethyl)amino]-2-propanol (0.18 g, 0.216 mmol) was reacted according to Procedure H (eluant: 10:1 going to 5:1 chloroform-methanol containing 1% ammonium hydroxide) to give the title compound (0.08 g, 0.134 mmol).

Sources & evidence

ORD record
ord-d0281eefaf4043d888d08f3430e0a64e
Source dataset
uspto-grants-2003_03
Patent number
US06537994B2

Reaction notes

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