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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388805Generated: October 30, 2026

Trifluoroacetic acid → HCID 66810863, compound

https://huagongshe.com/reaction/388805

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 numberUS08377964B2
Source datasetuspto-grants-2013_02
ORD IDord-ddedd7bc75f74e90819ed6e8cec6e077
Source noteuspto-grants-2013_02