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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374970Generated: October 26, 2026

3-Bromothiophene-2-carboxylic acid → 3-bromo-N-[1-(3-{[4-(methyloxy)phenyl]amino}1,2,4-triazin-6-yl)ethyl]-2-thiophenecarboxamide

https://huagongshe.com/reaction/2374970

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromothiophene-2-carboxylic acidHCID 2739688—
Reactant5-bromo-N-[1-(3-{[4-(methyloxy)phenyl]amino}-1,2,4-triazin-6-yl)ethyl]-2-thiophenecarboxamideHCID 58711930—
Reactant6-(1-aminoethyl)-N-[4-(methyloxy)phenyl]-1,2,4-triazin-3-amineHCID 58711999—
Product3-bromo-N-[1-(3-{[4-(methyloxy)phenyl]amino}1,2,4-triazin-6-yl)ethyl]-2-thiophenecarboxamideHCID 58711983—

Reaction Steps

In a similar manner as described for Intermediate 48, using 6-(1-aminoethyl)-N-[4-(methyloxy)phenyl]-1,2,4-triazin-3-amine (Intermediate 47) (100 mg, 0.41 mmol), and 3-bromothiophene-2-carboxylic acid (93 mg, 0.45 mmol), except the reaction was stirred for 6.5 h and purification using silica SPE was omitted, to give 3-bromo-N-[1-(3-{[4-(methyloxy)phenyl]amino}1,2,4-triazin-6-yl)ethyl]-2-thiophenecarboxamide (162 mg) as a yellow solid. MS m/z 434/436 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462614B2
Source datasetuspto-grants-2008_12
ORD IDord-6ff0d1a8a2f5499ca18ab7be59c7c66b
Source noteuspto-grants-2008_12