HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896358Generated: October 30, 2026
Acetyl chloride → HCID 20813993, compound
https://huagongshe.com/reaction/896358
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 69719649 | HCID 69719649 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20813993 | HCID 20813993 | — |
Reaction Steps
To a suspension of [2-[2,4-dioxo-3-(2,2,2-trifluoro-ethyl)-3,4-dihydro-2H-quinazolin-1-ylmethyl]-1-(4-hydroxy-butyl)-1H-benzoimidazol-5-ylmethyl]-carbamic acid tert-butyl ester (80 mg, 0.14 mmol) in dichloromethane (3 mL) was added TFA (319 μL, 4.14 mmol). The solution was allowed to stir for 6 hrs. followed by the removal of the volatiles in vacuo. The resulting trifluoroacetate was dissolved in methanol (3 mL) followed by the addition of acetyl cloride (98 μL, 1.4 mmol) and concentrated after 10 min. This procedure was repeated once allowing the reaction to run for 3 hrs. The solution was concentrated in vacuo and the residue stripped with DCM (thrice). The product was triturated in diethyl ether and the ether decanted to yield 1-[5-Aminomethyl-1-(4-hydroxy-butyl)-1H-benzoimidazol-2-ylmethyl]-3-(2,2,2-trifluoro-ethyl)-1H-quinazoline-2,4-dione; HCl salt (79 mg, 100%) as a white solid:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06919331B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-80656de0bb944c5aab30b3a546253ab8 |
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| Source note | uspto-grants-2005_07 |
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