2-Amino-4-methylthiazole → HCID 16117058, compound

HRID 1787636Notes

Reaction equation

HRID 1787636 reaction equation
Cl[C:2]1[N:3]=[CH:4][C:5](I)=[C:6]2[C:11]=1[N:10]=[C:9]([CH3:12])[CH:8]=[CH:7]2.[F:14][C:15]1[CH:16]=[N:17][CH:18]=[C:19](B(O)O)[CH:20]=1.[NH2:24][C:25]1[S:26][CH:27]=[C:28]([CH3:30])[N:29]=1>>[F:14][C:15]1[CH:20]=[C:19]([C:5]2[CH:4]=[N:3][C:2]([NH:24][C:25]3[S:26][CH:27]=[C:28]([CH3:30])[N:29]=3)=[C:11]3[C:6]=2[CH:7]=[CH:8][C:9]([CH3:12])=[N:10]3)[CH:18]=[N:17][CH:16]=1

Participants

4

Reactant 3

HCID 741432-Amino-4-methylthiazoleHCID 44717403(5-Fluoropyridin-3-yl)boronic acidHCID 576003528-Chloro-5-iodo-2-methyl-[1,7]naphthyridine

Product 1

HCID 16117058HCID 16117058, compound

Procedure

The title compound, MS: m/e=352.2 (M+H+), was prepared in accordance with the general method of example 15 step 1 and step 3 from 8-chloro-5-iodo-2-methyl-[1,7]naphthyridine (Example I), 3-fluoro-5-pyridineboronic acid and 2-amino-4-methylthiazole.

Sources & evidence

ORD record
ord-4e6b8d0055844665bae77ba5f661a749
Source dataset
uspto-grants-2009_03
Patent number
US07511055B2

Reaction notes

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