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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489667Generated: October 29, 2026

Trifluoroacetic acid → HCID 10210143, compound

https://huagongshe.com/reaction/489667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 3-(n-[(1r)-1-[(4-chlorophenyl)methyl]-2-(4-{2-[(cyclopropylmethyl)-(methylsulfonyl)amino]phenyl}piperidyl)-2-oxoethyl]carbamoyl)azetidine-carboxylateHCID 23587442—
SolventDichloromethaneHCID 6344—
ProductHCID 10210143HCID 10210143—

Reaction Steps

The title compound was prepared according to the procedure described in Example 3 (Step b) using tert-butyl 3-(N-[(1R)-1-[(4-chlorophenyl)methyl]-2-(4-{2-[(cyclopropylmethyl)-(methylsulfonyl)amino]phenyl}piperidyl)-2-oxoethyl]carbamoyl)azetidine-carboxylate (Step a) (565 mg, 0.84 mmol) and 50% TFA in CH2Cl2 (6 mL). Purification by reverse phase preparative HPLC [YMC-Pack ODS-AM 250×20 mm 5 μm column, 40% to 75% CH3CN (0.1% TFA) in H2O(0.1% TFA) over 10 min] provided the title compound (TFA salt) as an amorphous white solid (420 mg). MS (ESI, pos. ion) m/z: 573 (M+1). Calcd for C29H37ClN4O4S: 572.22. Anal. Calcd for C29H37ClN4O4S 1.7C2HF3O2: C, 50.74; H, 5.09; N, 7.30, S, 4.18. Found: C. 50.47; H, 5.03; N, 7.36; S, 4.28.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06977264B2
Source datasetuspto-grants-2005_12
ORD IDord-8d99ee1763064ad49cd457810cb25a95
Source noteuspto-grants-2005_12