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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628890Generated: October 30, 2026

Acetic Anhydride → HCID 57786245, compound

https://huagongshe.com/reaction/1628890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 57786347HCID 57786347—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57786245HCID 5778624541.5%

Reaction Steps

To a mixture of 1-(2,4-dichlorophenyl)-N7,N7-diethyl-2,3,4,5-tetrahydro-1H-[1,3]diazepino[1,2-a]benzimidazole-4,7-diamine (59.5 mg, 0.142 mmol) and triethylamine (0.0396 mL, 0.284 mmol) in tetrahydrofuran (1.4 mL) was added acetic anhydride (0.161 mL, 0.170 mmol) at 0° C. After the resultant mixture was stirred at 0° C. for 1 hr, aqueous sodium bicarbonate was added and the mixture was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with a 50-100% ethyl acetate/n-hexane gradient mixture to give a solid, which was recrystallized from ethyl acetate to afford the title compound as a colorless solid (27.1 mg, 0.0589 mmol, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785460B2
Source datasetuspto-grants-2014_07
ORD IDord-e62c8b9e3c7d4d5f8435b0b418f42c65
Source noteuspto-grants-2014_07