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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899368Generated: October 29, 2026

Acetic Anhydride → HCID 5280203, compound

https://huagongshe.com/reaction/899368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 5280149HCID 5280149—
SolventPyridineHCID 1049—
ProductHCID 5280203HCID 528020369%

Reaction Steps

1-(benzoyl)-4-[(4-methoxy-7-(2-amino-pyrazin-5-yl)-6-azaindol-3-yl)-oxoacetyl]piperazine (4 mg) and acetic anhydride (20 mg) were dissolved in pyridine (0.5 ml). The reaction was stiffed for three hours at room temperature. After reaction was quenched with MeOH (1 ml), solvents were concentrated to give a residue which was purified using a Shimadzu automated preparative HPLC System to provide 3.0 mg of the desired compound, 1-(benzoyl)-4-[(4-methoxy-7-(2-acetylamino-pyrazin-5-yl)-6-azaindol-3-yl)-oxoacetyl]piperazine. 1H NMR (500 MHz, CD3OD) δ9.58 (s, 1H), 9.25 (s, 1H), 8.45 (s, 1H), 8.10 (s, 1H), 7.49 (m, 5H), 4.12 (s, 3H), 3.84-3.35 (m, 8H), 2.27 (s, 3H). MS m/z: (M+H)+ Calc'd for C27H26N7O5: 528.20; found 528.22. HPLC retention time: 1.33 minutes (column A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07354924B2
Source datasetuspto-grants-2008_04
ORD IDord-156924a88b024feca43423647b1cc191
Source noteuspto-grants-2008_04