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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443882Generated: November 1, 2026

Acetic Anhydride → HCID 5280203, compound

https://huagongshe.com/reaction/1443882

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 stirred 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 numberUS07662823B2
Source datasetuspto-grants-2010_02
ORD IDord-062f75c8e6f54377be2ce133bf607476
Source noteuspto-grants-2010_02