HCID 66955902, compound → HCID 66955959, compound

HRID 1399773Notes

Reaction equation

HRID 1399773 reaction equation
C(OC(C1C(C)=NC(N2CCCCC2)=NC=1C1C=CC(C)=CC=1)C(OC)=O)(C)(C)C.[C:31]([O:35][CH:36]([C:41]1[C:42]([C:54]([CH3:57])([CH3:56])[CH3:55])=[N:43][C:44]([N:48]2[CH2:53][CH2:52][CH2:51][CH2:50][CH2:49]2)=[N:45][C:46]=1[CH3:47])[C:37]([O:39]C)=[O:38])([CH3:34])([CH3:33])[CH3:32]>>[C:31]([O:35][CH:36]([C:41]1[C:42]([C:54]([CH3:57])([CH3:56])[CH3:55])=[N:43][C:44]([N:48]2[CH2:49][CH2:50][CH2:51][CH2:52][CH2:53]2)=[N:45][C:46]=1[CH3:47])[C:37]([OH:39])=[O:38])([CH3:33])([CH3:34])[CH3:32]

Participants

3

Reactant 2

HCID 66955902HCID 66955902, compoundHCID 66956235HCID 66956235, compound

Product 1

HCID 66955959HCID 66955959, compound

Procedure

This compound is prepared following the same procedure as described for example 185 wherein methyl 2-tert-butoxy-2-(4-methyl-2-(piperidin-1-yl)-6-p-tolylpyrimidin-5-yl)acetate is replaced by methyl 2-tert-butoxy-2-(4-tert-butyl-6-methyl-2-(piperidin-1-yl)pyrimidin-5-yl)acetate.

Workup

  1. customThis compound is prepared

Sources & evidence

ORD record
ord-29dba328c12f434b890f136359df4667
Source dataset
uspto-grants-2014_12
Patent number
US08906906B2

Reaction notes

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