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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748304Generated: October 31, 2026

Trifluoroacetic acid → HCID 67235165, compound

https://huagongshe.com/reaction/1748304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67237067HCID 67237067—
SolventDichloromethaneHCID 6344—
ProductHCID 67235165HCID 67235165—

Reaction Steps

TFA (60 mL) is added to a solution of crude diethyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}tetrahydro-2H-pyran-4-yl)methyl]-1H-indole-2,6-dicarboxylate from the preceding step in CH2Cl2 (400 mL). The reaction mixture is stirred at room temperature for 2 h. Then the solvent is removed under vacuum and the residue is dissolved in EtOAc (300 mL) and washed with saturated NaHCO3 solution until the pH is about 7. The aqueous layer is separated and it is extracted with EtOAc (100 mL). The organic layers are combined, dried over Na2SO4 and concentrated to afford the crude title compound which is used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150577B2
Source datasetuspto-grants-2015_10
ORD IDord-e27fdfecd98247fc981fe365b1915a1d
Source noteuspto-grants-2015_10