HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102313Generated: October 28, 2026
Trifluoroacetic acid → HCID 11338795, compound
https://huagongshe.com/reaction/2102313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 69003859 | HCID 69003859 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11338795 | HCID 11338795 | 70.9% |
Reaction Steps
Trifluoroacetic acid (0.5 mL) was added to a solution of 8-[3-(3-chloro-phenyl) -[1,2,4]oxadiazol-5-yl]-3-(4-methoxy-phenyl)-5,6-dihydro-8H-[1,2,4]triazolo[4,3-a]pyrazine-7-carboxylic acid tert-butyl ester (72.5 mg, 0.14 mmol) in dichloromethane (1 mL) at 0° C. The reaction mixture was then diluted with dichloromethane, After 15 minutes, the reaction was warmed to room temperature and stirred for an additional hour. washed with saturated sodium bicarbonate, dried over anhydrous sodium sulfate, filtered and concentrated. Purification was performed by flash column chromatography on silica gel using 85-90% ethyl acetate in hexanes to 2% ammonia in methanol in dichloromethane followed by trituration with diethyl ether to afford the titled compound (40.6 mg, 69%). 1H NMR (CDCl3) δ (ppm): 8.10 (m, 1H), 8.00 (m, 1H), 7.67 (m, 2H), 7.48 (m, 2H), 7.05 (m, 2H), 7.86 (m, 1H), 4.09 (m, 3H), 3.89 (s, 3H), 3.47 (m, 2H), 3.24 (m, 1H), 2.83 (bs, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07576077B2 |
|---|
| Source dataset | uspto-grants-2009_08 |
|---|
| ORD ID | ord-26e6c7bcca3d44d89f05ffd3f4e2b449 |
|---|
| Source note | uspto-grants-2009_08 |
|---|