HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623768Generated: October 30, 2026
Trifluoroacetic acid → HCID 73295489, compound
https://huagongshe.com/reaction/623768
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86711853 | HCID 86711853 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 73295489 | HCID 73295489 | — |
Reaction Steps
To tert-butyl 4-(1-benzyl-3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-2-carbonyl)-2,2-dimethylpiperazine-1-carboxylate (103 mg, 0.178 mmol) in DCM (2 mL) was added TFA (0.234 mL, 3.03 mmol). The reaction mixture was stirred for 1 h and then cooled to 0° C. Saturated aqueous NaHCO3 (15 mL) was added. The aqueous layer was separated and extracted twice with DCM (10 mL). The combined organic phases were washed with brine (20 mL) and dried over Na2SO4. Concentration in vacuo was followed by flash chromatography (silica, gradient heptane/EtOAc, 1:0→0:1). Appropriate fractions were combined, solvents removed in vacuo and the product was placed with MeOH (5 mL) in a vial. The remaining oil was dried in vacuo at 40° C. over 6 h. SC-82 (58 mg, 67%) was obtained as a white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09302988B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-03b876a32c904b13b821fa82b9934b24 |
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| Source note | uspto-grants-2016_04 |
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