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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356774Generated: October 31, 2026

Trifluoroacetic acid → HCID 66810863, compound

https://huagongshe.com/reaction/2356774

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 numberUS07759363B2
Source datasetuspto-grants-2010_07
ORD IDord-c0797d02b337487a84f2701f3d4dbf76
Source noteuspto-grants-2010_07