HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362634Generated: November 1, 2026
Trifluoroacetic acid → HCID 67002707, compound
https://huagongshe.com/reaction/2362634
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 67003360 | HCID 67003360 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67002707 | HCID 67002707 | — |
Reaction Steps
To an ambient solution of 4-(4-(5-chloro-4-(2-(3-(4-methoxybenzyloxy)oxetan-3-yl)thiazol-5-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridin-2-yl)benzyl)morpholine (Example 11H) (130 mg, 0.172 mmol) in dichloromethane (2.5 mL) was added trifluoroacetic acid (2.5 mL, 32.4 mmol). The reaction was stirred for 0.5 hours and was then concentrated to dryness under reduced pressure. The residue was partitioned between ethyl acetate (5 mL) and saturated aqueous bicarbonate solution (1 mL). The layers were separated, and the organic layer was dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel, eluting with a gradient of 0 to 10% methanol in dichloromethane, to give the title compound. MS ESI(+) m/z 637.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691810B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-81a69ff94a1245c3ad83b37258a9f0a7 |
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| Source note | uspto-grants-2014_04 |
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