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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571112Generated: November 1, 2026

Trifluoroacetic acid → HCID 67449901, compound

https://huagongshe.com/reaction/571112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67455917HCID 67455917—
SolventDichloromethaneHCID 6344—
ProductHCID 67449901HCID 67449901—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (4-(tert-butoxycarbonyl)aminonaphthalen-1-yl)(2-(tert-butoxycarbonyl)amino pyridin-4-yl)methane (270 mg, 0.60 mmol) in dry DCM (6.0 mL) under N2 at 0° C. was added TFA (2.0 mL, 25 mmol). The reaction was maintained at 0° C. for a further 20 min and was then warmed to RT for 4 hr. The mixture was evaporated in vacuo and the residue was subjected to SCX capture and release to afford the title compound, Intermediate H1, (150 mg, 100%); Rt 0.79 min (Method 2); m/z 250 (M+H)+ (ES+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024041B2
Source datasetuspto-grants-2015_05
ORD IDord-15c313b1b76340f28863d697bfe76e3c
Source noteuspto-grants-2015_05