2-Aminopyridine → HCID 12450085, compound

HRID 1415671Notes

Reaction equation

[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]=[C:9]=[S:10])=[CH:4][CH:3]=1.[NH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][N:13]=1>>[N:13]1[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=1[NH:11][C:9]([NH:8][C:5]1[CH:6]=[CH:7][C:2]([Br:1])=[CH:3][CH:4]=1)=[S:10]

Participants

Reactant 2

HCID 104392-Aminopyridine

HCID 161334-Bromophenyl isothiocyanate

Product 1

HCID 12450085HCID 12450085, compound

Procedure

The title compound was synthesized according to the procedure in Example 8 by employing 4-bromophenyl isothiocyanate instead of phenyl isothiocyanate and 2-aminopyridine instead of 4-methyl-2-aminopyridine.

Sources & evidence

ORD record: ord-9ee591a32d364a8e99b3338416c010e4
Source dataset: uspto-grants-1999_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05908842

Reaction notes

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