HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170150Generated: October 30, 2026
Trifluoroacetic acid → HCID 78323679, compound
https://huagongshe.com/reaction/2170150
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 90386205 | HCID 90386205 | — |
| Product | HCID 78323679 | HCID 78323679 | 26% |
Reaction Steps
N-(tert-Butyl)-4-(5-phenyl-4-((pyridin-2-ylmethyl)amino)pyrrolo[2,1-f][1,2,4]triazin-2-yl)thiazole-2-sulfonamide (40.0 mg, 0.0770 mmol) and TFA (3 mL) were stirred at ambient temperature for 14 h. The excess TFA was evaporated under reduced pressure and the residue purified by preparative HPLC (Condition B-33 as described in general methods) to obtain 4-(5-phenyl-4-((pyridin-2-ylmethyl)amino)pyrrolo[2,1-f][1,2,4]triazin-2-yl)thiazole-2-sulfonamide (9.00 mg, 26.0%). LCMS Condition B-13: retention time 1.94 min, [M+1]=464.0. HPLC Condition B-32: retention time 7.06 min, Purity 97.62%. 1H NMR (400 MHz, DMSO-d6): δ ppm 4.91 (d, J=4.4 Hz, 2H), 6.82 (d, J=2.8 Hz, 1H), 7.27-7.31 (m, 2H), 7.43-7.61 (m, 6H), 7.79 (dt, J=2.0 Hz, J=8.0 Hz, 1H), 7.90 (d, J=2.8 Hz, 1H), 8.24 (s, 2H), 8.39-8.40 (m, 1H), 8.63 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09050345B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-2b268e5b67d645eba22883aef71f55e2 |
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| Source note | uspto-grants-2015_06 |
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