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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172802Generated: November 2, 2026

Acetic Anhydride → HCID 87541472, compound

https://huagongshe.com/reaction/1172802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2-(4-{5-[(6,7-Dichloro-1-oxo-1,2-dihydropyrrolo[1,2-a]pyrazin-4-yl)methyl]-2-fluorobenzoyl}-1,4-diazepan-1-yl)ethanaminium trifluoroacetateHCID 87540407—
SolventPyridineHCID 1049—
ProductHCID 87541472HCID 87541472—

Reaction Steps

To a solution of Example 20, T1 in pyridine (0.15 M) was added Ac2O (1 eq) and the resulting mixture stirred overnight at RT. The solvent was evaporated under reduced pressure and the residue was purified at the prep RP-HPLC using H2O (+0.1% TFA) and MeCN (+0.1% TFA) as eluents (C18 column), the desired fractions were lyophilized to afford the titled compound as yellow powder. 1H NMR (300 MHz, DMSO-d6) δ: 10.97 (1H, d, J=5.6 Hz), 9.51 (1H, br. S), 8.22-8.16 (1H, m), 7.37-7.26 (3H, m), 7.20 (1H, s), 6.66-6.61 (1H, m), 4.42 (2H, s), 4.10 (1H, m), 3.63-3.14 (11H, m), 2.11 (1H, m), 1.95-1.88 (4H, m). MS (ES) C24H26Cl2FN5O3 required: 521, found: 522 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834015B2
Source datasetuspto-grants-2010_11
ORD IDord-233fee2b81824391b66e08995c89dc8d
Source noteuspto-grants-2010_11