Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606392Generated: October 30, 2026

1-Hydroxybenzotriazole → 6-cyano-4-oxo-N-[[3-[[[2-(1H-1,2,4-triazol-5-yl)acetyl]amino]methyl]phenyl]methyl]-1H-quinazoline-2-carboxamide

https://huagongshe.com/reaction/606392

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN-{[3-(aminomethyl)phenyl]methyl}-6-cyano-4-oxo-3,4-dihydroquinazoline-2-carboxamide hydrochlorideHCID 136380963—
Reactant2-(1H-1,2,4-triazol-3-yl)acetic acidHCID 178525244—
SolventDimethylformamideHCID 6228—
Product6-cyano-4-oxo-N-[[3-[[[2-(1H-1,2,4-triazol-5-yl)acetyl]amino]methyl]phenyl]methyl]-1H-quinazoline-2-carboxamideHCID 17850949524%

Reaction Conditions

Temperature40 °C

Reaction Steps

A solution of N-{[3-(aminomethyl)phenyl]methyl}-6-cyano-4-oxo-3,4-dihydroquinazoline-2-carboxamide hydrochloride obtained in Reference Example 47 (170 mg, 0.460 mmol), 1H-1,2,4-triazol-3-ylacetic acid obtained in Reference Example 15 (70.0 mg, 0.551 mmol), diisopropylethylamine (0.079 mL, 0.460 mmol), 1-[3-(dimethylamino)propyl]-3-ethyl-carbodiimide hydrochloride (106 mg, 0.550 mmol) and 1-hydroxybenzotriazole (74.0 mg, 0.550 mmol) in DMF (10 mL) was stirred at 40° C. for 15 hr. The reaction mixture was concentrated under reduced pressure, and water was added to the residue. The resulting solid was collected by filtration, washed with water and IPE, and dried. The obtained crude crystals were recrystallized from ethyl acetate-IPE to give the title compound as a white powder (49.4 mg, 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915267B2
Source datasetuspto-grants-2011_03
ORD IDord-820bbeeb5ece489db2ba65d41f3015d6
Source noteuspto-grants-2011_03