HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899368Generated: October 29, 2026
Acetic Anhydride → HCID 5280203, compound
https://huagongshe.com/reaction/899368
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 5280149 | HCID 5280149 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 5280203 | HCID 5280203 | 69% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07354924B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-156924a88b024feca43423647b1cc191 |
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| Source note | uspto-grants-2008_04 |
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