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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098343Generated: November 1, 2026

Trifluoroacetic acid → HCID 66810863, compound

https://huagongshe.com/reaction/1098343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 66810908HCID 66810908—
SolventDichloromethaneHCID 6344—
ProductHCID 66810863HCID 6681086388%

Reaction Steps

Crude 4-(4-{[(2-tert-butyl-1H-benzoimidazole-4-carbonyl)amino]methyl}-piperidin-1-ylmethyl)piperidine-1-carboxylic acid tert-butyl ester, prepared as in the previous step (5.1 g, 10 mmol) was treated with a mixture of trifluoroacetic acid (40 mL) and dichloromethane (40 mL) at room temperature for 0.5 h. The mixture was concentrated in vacuo, redissolved in dichloromethane (25 mL) and basified with 1M aqueous sodium hydroxide (15 mL). The organic layer was removed, and the aqueous layer re-extracted with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered, and concentrated in vacuo to afford the desired product as a brown foam (3.6 g, 8.8 mmol, 88%). (m/z): [M+H]+ calcd for C24H37N5O 412.31, found 412.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143279B2
Source datasetuspto-grants-2012_03
ORD IDord-a27ae2c3165e462ebcff6c1b14fe52ba
Source noteuspto-grants-2012_03