Ethyl Acetoacetate → ethyl 4-amino-2-methyl-5-((tetrahydro-2H-pyran-4-yl)oxy)quinoline-3-carboxylate

HRID 2047866Notes

Reaction equation

[NH2:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([O:10][CH:11]2[CH2:16][CH2:15][O:14][CH2:13][CH2:12]2)[C:3]=1[C:4]#[N:5].O=[C:18]([CH3:25])[CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21]>>[CH2:23]([O:22][C:20]([C:19]1[C:18]([CH3:25])=[N:1][C:2]2[C:3]([C:4]=1[NH2:5])=[C:6]([O:10][CH:11]1[CH2:16][CH2:15][O:14][CH2:13][CH2:12]1)[CH:7]=[CH:8][CH:9]=2)=[O:21])[CH3:24]

Participants

Reactant 2

HCID 8868Ethyl Acetoacetate

HCID 667459382-amino-6-((tetrahydro-2H-pyran-4-yl)oxy)benzonitrile

Product 1

HCID 66746015ethyl 4-amino-2-methyl-5-((tetrahydro-2H-pyran-4-yl)oxy)quinoline-3-carboxylate

Procedure

Prepared as in Example 2a from 2-amino-6-((tetrahydro-2H-pyran-4-yl)oxy)benzonitrile (Example 118b) and ethyl 3-oxobutanoate as a pale yellow solid (51%). MS 331 (MH+).

Sources & evidence

ORD record: ord-c8f2d1702cf344d190eefd810f60dd34
Source dataset: uspto-grants-2013_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08592592B2

Reaction notes

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