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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504139Generated: November 1, 2026

Acetic Acid → HCID 70656505, compound

https://huagongshe.com/reaction/1504139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-(4-methylthiazol-5-ylmethyl)-N-(2-pyridin-3-ylethyl)amineHCID 65721669—
Reactant1-ethyl-3,3,5-trimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepine-7-carbaldehydeHCID 86670476—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 70656505HCID 7065650548.8%

Reaction Steps

1-Ethyl-3,3,5-trimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepine-7-carbaldehyde(0.423 g) and acetic acid(0.14 g) were added to a 1,2-dichloroethane solution (10 ml) of N-(4-methylthiazol-5-ylmethyl)-N-(2-pyridin-3-ylethyl)amine(0.36 g). The mixture was stirred at room temperature for 30 minutes. Sodium triacetoxyborohydride(0.48 g) was added, and the mixture was stirred at room temperature overnight. The reaction liquid was condensed under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate: methanol=100:0→50:50). The purified product was condensed under reduced pressure. The residue was washed with diethyl ether, and dried to give the title compound(0.37 g) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212187B2
Source datasetuspto-grants-2015_12
ORD IDord-c7645ad0a9b04c88a3fe49ee88ab57d8
Source noteuspto-grants-2015_12