HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874396Generated: October 29, 2026
3-(Trifluoromethyl)benzoyl chloride → HCID 45381324, compound
https://huagongshe.com/reaction/874396
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(Trifluoromethyl)benzoyl chloride | HCID 75257 | — |
| Reactant | HCID 58506753 | HCID 58506753 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 45381324 | HCID 45381324 | — |
Reaction Steps
A solution of (S)-tert-butyl 3-(4-amino-3-(4-aminophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)pyrrolidine-1-carboxylate (0.075 g, 0.17 mmol) in CH2Cl2 (10 mL) was cooled in an ice-water bath. To this, 3-(trifluoromethyl)benzoyl chloride (0.025 mL, 0.17 mmol) diluted in CH2Cl2 (5 mL) was added dropwise. The reaction was allowed to warm to room temperature and left stirring for 4 hours, yielding the benzamide derivative (ESI-MS m/z [M+H]+ found 568.5, calculated 568.6). Boc-deprotection was completed through the addition of formic acid (5 mL) and concentrated HCl (0.5 mL) added dropwise directly to the reaction mixture. The reaction mixture was left stirring for 12 hours and then was concentrated in vacuo, resuspended in 50:50 H2O—CH3CN, and purified on a C18 column in CH3CN/H2O/0.1% TFA (1-100% gradient) to afford AD70. ESI-MS m/z [M+H]+ found 468.5, calculated 468.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08980899B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-706762909c62434a8fc894bac4b7692f |
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| Source note | uspto-grants-2015_03 |
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