Urea → HCID 57424692, compound

HRID 1093280Notes

Reaction equation

NC(N)=O.[CH:5]12[O:12][CH:9](CC1)[CH2:8][N:7]([C:13]1[N:18]=[C:17]([C:19]3[CH:24]=[CH:23][C:22]([NH:25][C:26]([NH:28][CH2:29][CH3:30])=[O:27])=[CH:21][CH:20]=3)[N:16]=[C:15]3[N:31]([CH:34]4CCN(C(OCC)=O)C[CH2:35]4)[N:32]=[CH:33][C:14]=13)[CH2:6]2.[CH3:45][N:46]([CH2:48][C:49]1[CH:55]=CC(N)=[CH:51][CH:50]=1)[CH3:47].N[C:57]1C=CC=C[CH:58]=1>>[CH:6]12[N:7]([C:13]3[N:18]=[C:17]([C:19]4[CH:20]=[CH:21][C:22]([NH:25][C:26]([NH:28][C:29]5[CH:51]=[CH:50][C:49]([CH2:48][N:46]([CH3:47])[CH3:45])=[CH:55][CH:30]=5)=[O:27])=[CH:23][CH:24]=4)[N:16]=[C:15]4[N:31]([CH2:34][CH3:35])[N:32]=[CH:33][C:14]=34)[CH:8]([CH2:57][CH2:58]1)[CH2:9][O:12][CH2:5]2

Participants

Reactant 4

HCID 1176Urea

HCID 6115Aniline

HCID 308051Benzenemethanamine, 4-amino-N,N-dimethyl-

HCID 25262323ethyl 4-(4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-(4-(3-ethylureido)phenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidine-1-carboxylate

Product 1

HCID 57424692HCID 57424692, compound

Procedure

A urea formation procedure similar to that used for the synthesis of ethyl 4-(4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-(4-(3-ethylureido)phenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidine-1-carboxylate is used, utilizing 4-((dimethylamino)methyl)aniline as the aniline component. (23%, MS=527.2 (M+H))

Sources & evidence

ORD record: ord-747a28d98e6b46ed9c15e5809f8f47a3
Source dataset: uspto-grants-2012_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08129371B2

Reaction notes

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