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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481067Generated: October 30, 2026

Acetic Acid → HCID 20605631, compound

https://huagongshe.com/reaction/481067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantChloroformHCID 6212—
ReactantSodium hydrideHCID 24758—
ReactantHCID 20605627HCID 20605627—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 20605631HCID 20605631—

Reaction Steps

To a solution of 6-[2-(4-Nitro-phenyl)-ethyl]-5,6-dihydro-4H-1,3a,6-triaza-as-indacene-8-carboxylic acid methyl ester (19.67 mmol) in 100 mL DMF is treated with sodium hydride (60%, 1.97 g, 49.18 mmol) portion wise. The reaction is complete in about 2 h at 20° C. Chloroform is added and the reaction mixture is cooled to 5° C. before the dropwise addition of acetic acid (3.15 mL, 55.08 mmol) until pH of 1-3. A saturated solution of aqueous KHCO3 (150 mL) is added, stirred and separated. The separated organic phase is washed with water twice. The filtrate is concentrated directly. Most of the DMF is removed by high vacuum to give a brown wet solid. The wet solid is cooled to room temp. Ether is added, stirred, and filtered to give a brown solid which is dried in air overnight to give 5,6-dihydro-4H-1,3a,6-triaza-as-indacene-8-carboxylic acid methyl ester, 9.11 g, (77%): 1H NMR (CD3OD) 3.05 (t, 2H), 3.86 (s, 3H), 4.25 (t, 2H), 6.97 (s, 1H), 7.05 (s, 1H), 7.40 (s, 1H); LRMS calcd 217.23, found [M−H] 216.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06653471B2
Source datasetuspto-grants-2003_11
ORD IDord-884a00b6d574413e9214af7d7a00d295
Source noteuspto-grants-2003_11