HCID 178455253, compound → HCID 178519973, compound

HRID 2169528Notes

Reaction equation

OCCN(C)C(C1C(OCC2C=CC=CC=2)=C(O)N=C(CC2(C3C4C(=CC=CC=4)C=CC=3)CCCC2)N=1)=O.[CH2:39]([N:46]([CH2:77][CH2:78][O:79][Si](C(C)(C)C)(C)C)[C:47]([C:49]1[C:54]([O:55][CH2:56][C:57]2[CH:62]=[CH:61][CH:60]=[CH:59][CH:58]=2)=[C:53]([OH:63])[N:52]=[C:51]([CH2:64][C:65]2([C:70]3[CH:75]=[CH:74][C:73]([Cl:76])=[CH:72][CH:71]=3)[CH2:69][CH2:68][CH2:67][CH2:66]2)[N:50]=1)=[O:48])[C:40]1[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=1>>[CH2:39]([N:46]([CH2:77][CH2:78][OH:79])[C:47]([C:49]1[C:54]([O:55][CH2:56][C:57]2[CH:62]=[CH:61][CH:60]=[CH:59][CH:58]=2)=[C:53]([OH:63])[N:52]=[C:51]([CH2:64][C:65]2([C:70]3[CH:75]=[CH:74][C:73]([Cl:76])=[CH:72][CH:71]=3)[CH2:66][CH2:67][CH2:68][CH2:69]2)[N:50]=1)=[O:48])[C:40]1[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=1

Participants

Reactant 2

HCID 178455253HCID 178455253, compound

HCID 178484637HCID 178484637, compound

Product 1

HCID 178519973HCID 178519973, compound

Procedure

This compound was prepared following the same method as described for 5-benzyloxy-6-hydroxy-2-(1-naphthalen-1-yl-cyclopentylmethyl)-pyrimidine-4-carboxylic acid (2-hydroxyethyl)-methyl-amide (351) from N-benzyl-5-(benzyloxy)-N-(2-((tert-butyldimethylsilyl)oxy)ethyl)-2-((1-(4-chlorophenyl)cyclopentyl)methyl)-6-hydroxypyrimidine-4-carboxamide (506).

Workup

customThis compound was prepared

Sources & evidence

ORD record: ord-26e07f84060a481a95999079f0fd6d9b
Source dataset: uspto-grants-2015_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09045486B2

Reaction notes

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