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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44224Generated: October 29, 2026

Acetic Acid → 4-(9H-benzo[f]pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepin-3-yl)benzoic acid

https://huagongshe.com/reaction/44224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantLithium HydroxideHCID 3939—
Reactantmethyl 4-(9H-benzo[f]pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepin-3-yl)benzoateHCID 136163852—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product4-(9H-benzo[f]pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepin-3-yl)benzoic acidHCID 136163762—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a suspension of methyl 4-(9H-benzo[f]pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepin-3-yl)benzoate (0.5 g, 1.4 mmol) in methanol (20 mL) was added lithium hydroxide (0.16 g, 6.8 mmol) and water (2 mL). The reaction mixture was stirred at 70° C. for 3 days. The reaction pH was acidified by the addition of acetic acid followed by ethyl acetate. The solid was filtered off and washed with water. The solid was re-suspended in ethyl acetate, stirred, filtered off and dried under vacuum. The 4-(9H-benzo[f]pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepin-3-yl)benzoic acid was obtained as a yellow solid (0.48 g, quantitative). M.p.>300° C.; 400 MHz 1H NMR (DMSO-d6) δ: 13.20 (br.s, 1H), 8.83 (br.s, 1H), 8.23 (d, J=4.4 Hz, 1H), 8.05-7.95 (m, 3H), 7.56 (d, J=8.0 Hz, 2H), 7.45 (t, J=4.9 Hz, 1H), 7.36 (d, J=8.0 Hz, 1H), 7.2-7.1 (m, 2H), 6.92 (dd, J=7.6, 4.4 Hz, 1H); LCMS [M+H]: 356.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541407B2
Source datasetuspto-grants-2013_09
ORD IDord-ebf8ac7db3f749ef887df238666bbdc2
Source noteuspto-grants-2013_09