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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836569Generated: November 3, 2026

Trifluoroacetic acid → HCID 68523991, compound

https://huagongshe.com/reaction/1836569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 23518419HCID 23518419—
SolventDichloromethaneHCID 6344—
ProductHCID 68523991HCID 6852399124.6%

Reaction Steps

To a solution of (±)-cis-tert-butyl 2-anilino-5,6,8a,9,11,11a-hexahydro-4H-pyrido[3,2,1-ij]pyrrolo[3,4-c]quinoline-10(8H)-carboxylate (80 mg, 0.20 mmol) in 5 ml of CH2Cl2 was added 1 ml of trifluoroacetic acid and the reaction was stirred at room temperature for 3 h. The volatiles were removed under reduced pressure and the residue was purified by prep HPLC (C18 reverse phase column, elution with a H2O/CH3CN gradient with 0.5% TFA). Product-containing fractions were combined, concentrated and partitioned between chloroform and saturated aqueous sodium carbonate. The organics were washed with brine, dried (K2CO3) and concentrated in vacuo to afford 15 mg (23%) of the title compound of EXAMPLE 17. 1H NMR (CDCl3): δ 7.18 (app t, 2H, J=7.8 Hz), 6.84 (app d, 2H, J=8.0 Hz), 6.78-6.72 (m, 1H), 6.67 (s, 1H), 6.65 (s, 1H), 5.46 (s, 1H), 3.45-3.30 (m, 2H), 3.24-3.17 (m, 1H), 3.08-3.00 (m, 2H), 2.97-2.85 (m, 1H), 2.78-2.55 (broad m, 6H), 2.05-1.93 (m, 2H). LRMS (ES)+: 306.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777406B2
Source datasetuspto-grants-2004_08
ORD IDord-1c2e47dc21e44d728938c8dcc2e45e53
Source noteuspto-grants-2004_08