HCID 58826993, compound → HCID 16119571, compound

HRID 502627Notes

Reaction equation

HRID 502627 reaction equation
[CH:1]([C:4]1[C:13]([O:14][C:15]2[C:16]([NH2:22])=[N:17][C:18]([NH2:21])=[N:19][CH:20]=2)=[CH:12][C:11]2[C:6](=[CH:7][CH:8]=[C:9](C)[CH:10]=2)[N:5]=1)([CH3:3])[CH3:2].C(C1C(OC2C(N)=NC(N)=NC=2)=CC2C(=C(C)C=CC=2)N=1)(C)C>>[CH:1]([C:4]1[C:13]([O:14][C:15]2[C:16]([NH2:22])=[N:17][C:18]([NH2:21])=[N:19][CH:20]=2)=[CH:12][C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=1)([CH3:3])[CH3:2]

Participants

3

Reactant 2

HCID 58826993HCID 58826993, compoundHCID 58827001HCID 58827001, compound

Product 1

HCID 16119571HCID 16119571, compound

Procedure

Similarly prepared were 5-(2-Isopropyl-6-methyl-quinolin-3-yloxy)-pyrimidine-2,4-diamine (MP=239.4-242.1° C.) and 5-(2-Isopropyl-8-methyl-quinolin-3-yloxy)-pyrimidine-2,4-diamine (MP=248.3-249.4° C.).

Workup

  1. customSimilarly prepared

Sources & evidence

ORD record
ord-5bbbea7b772749819687890939d13467
Source dataset
uspto-grants-2010_08
Patent number
US07776872B2

Reaction notes

Loading…