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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199784Generated: October 29, 2026

Trifluoroacetic acid → HCID 90220400, compound

https://huagongshe.com/reaction/2199784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 90220485HCID 90220485—
SolventDichloromethaneHCID 6344—
ProductHCID 90220400HCID 90220400102.3%

Reaction Steps

To a suspension of {1-[4-carbamoyl-5-(pyridin-2-ylamino)-thiazol-2-yl]-piperidin-3-yl}-carbamic acid tert-butyl ester (prepared as described in example 1) (359 mg, 0.86 mmol) in dichloromethane (10 mL) was added trifluoroacetic acid (10 mL, 130 mmol) to form a yellow solution. The mixture was stirred at ambient temperature for 30 minutes then evaporated to dryness in vacuo. The residue was taken up in dichloromethane (25 mL) and washed with saturated aqueous sodium hydrogen carbonate (100 mL). The organic layer was separated and the aqueous layer extracted with dichloromethane (5×20 mL) until no further yellow color was extracted in to the organic layer. The combined organic extracts were dried over sodium sulfate, filtered and concentrated in vacuo to give 2-((R)-3-amino-piperidin-1-yl)-5-(pyridin-2-ylamino)-thiazole-4-carboxylic acid amide as a yellow solid (280 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359345B2
Source datasetuspto-grants-2016_06
ORD IDord-8c75653b606543cf856fd8843f261380
Source noteuspto-grants-2016_06