2-Methoxyethanol → HCID 24961711, compound

HRID 1187262Notes

Reaction equation

C([NH:4][C:5]1[N:14]=[C:13](C2N=CNN=2)[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([C:20]3[CH:25]=[CH:24][C:23]([F:26])=[CH:22][CH:21]=3)[CH:11]=2)[N:6]=1)(=O)C.[CH3:27][O:28][CH2:29][CH2:30][OH:31]>>[NH2:4][C:5]1[N:14]=[C:13]([O:31][CH2:30][CH2:29][O:28][CH3:27])[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([C:20]3[CH:25]=[CH:24][C:23]([F:26])=[CH:22][CH:21]=3)[CH:11]=2)[N:6]=1

Participants

Reactant 2

HCID 80192-Methoxyethanol

HCID 178474428HCID 178474428, compound

Product 1

HCID 24961711HCID 24961711, compoundYield 84%

Procedure

This compound, synthesized from 2-acetamido-6-(4-fluorophenyl)-4-(1,2,4-triazolyl)-quinazoline and 2-methoxyethanol in 84% yield using the same procedure as in example 18, was characterized by its mass spectrum as follows: MS (m/z): 299 ([M+H]+, 100).

Sources & evidence

ORD record: ord-d61560bedbf34efe8299600941255e8f
Source dataset: uspto-grants-2014_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08673929B2

Reaction notes

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