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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73671Generated: October 28, 2026

Trifluoroacetic acid → HCID 57955254, compound

https://huagongshe.com/reaction/73671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 57955241HCID 57955241—
SolventDichloromethaneHCID 6344—
ProductHCID 57955254HCID 5795525493.3%

Reaction Steps

To a solution of CH2Cl2 (50 mL) was added of tert-butyl {4-[6-acetyl-4-amino-7-(morpholin-4-ylmethyl)pyrrolo[2,1-f][1,2,4]triazin-5-yl]-2 fluorophenyl}-carbamate (291 mg, 0.60 mmol) followed by trifluoroacetic acid (5 mL). The solution was allowed to stir for 30 min at rt. Aq saturated NaHCO3 was added to the solution until bubbling stopped. Additionally CH2Cl2 was added and the solution was then transferred to a separatory funnel. The organic layer was isolated while the aqueous layer was back extracted with CH2Cl2 (2×25 mL). The combined organic layers were collected, dried (MgSO4), filtered, and concentrated to dryness yielding 214 mg of the above compound as a white solid (0.56 mmol, yield 93%). 1H-NMR (DMSO-d6) δ 7.95 (s, 1H), 7.08 (dd, J=1.7 Hz, 10.3 Hz, 1H), 6.92 (dd, J=1.8 Hz, 7.9 Hz, 1H), 6.86 (t, J=8.7 Hz, 1H), 5.47 (s, 2H), 4.05 (s, 2H), 3.49 (m, 4H), 2.41 (m, 4H), 2.06 (s, 3H); MS [M+H]+=385.1; LCMS RT=1.16 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829185B2
Source datasetuspto-grants-2014_09
ORD IDord-f2855e6c6211402699751fb8b44ca782
Source noteuspto-grants-2014_09