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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386192Generated: October 30, 2026

Acetic Anhydride → HCID 11719868, compound

https://huagongshe.com/reaction/386192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 11517695HCID 11517695—
SolventDichloromethaneHCID 6344—
ProductHCID 11719868HCID 11719868—

Reaction Steps

1-(2-Phenyl-quinolin-7-yl)-3-piperidin-4-ylmethyl-imidazo[1,5-a]pyrazin-8-ylamine (100.00 mg, 0.23 mmol) in a dried 10 mL round-bottom flask was dissolved in 1.7 mL of methylene chloride and was charged with PS-DIEA (117.95 mg, 0.46 mmol). Acetic anhydride (Ac2O) (11 μL, 0.51 equiv) was added in one portion. After 15 min., another 5.5 μL of Ac2O (0.25 equiv) was added. After another 15 min., another 2.64 μL of Ac2O (0.12 equiv) was added. After another 15 min., another 11 μl of Ac2O (0.51 equiv) was added. The reaction was filtered through a fritted funnel, and the resins were rinsed multiple times with methylene chloride. The crude product was purified by silica gel flash chromatography (wetted with 100% EtOAc, eluted with 5% (7N NH3) in MeOH/EtOAc) and afforded the desired product; 1H NMR (400 MHz, CHLOROFORM-d) δ 8.41 (1 H, d, J=1.68), 8.28 (1 H, d, J=8.20), 8.19 (2 H, dd, J=1.51 Hz, J=1.18), 7.93 (3 H, m), 7.53 (3 H, m), 7.23 (1 H, d, J=5.10), 7.12 (1 H, d, J=5.76), 5.55 (2 H, m), 4.67 (1 H, d, J=13.28), 3.83 (1 H, d, J=12.26), 3.06 (1 H, m), 2.96 (2 H, m), 2.56 (1 H, m), 2.27 (1 H, m), 2.10 (3 H, s), 1.85 (2 H, t), 1.31 (2 H, m); MS (ES+): m/z 477.11/478.08 (40/20) [MH+]; HPLC: tR=2.11 min (OpenLynx, polar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367826B2
Source datasetuspto-grants-2013_02
ORD IDord-f82bd298d6f5491a8ce23fddf69ce75c
Source noteuspto-grants-2013_02