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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697555Generated: November 1, 2026

Isopropyl Acetate → HCID 59543587, compound

https://huagongshe.com/reaction/1697555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl AcetateHCID 7915—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(Trifluoromethyl)cyclopropane-1-carboxylic acidHCID 2778306—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 86646818HCID 86646818—
SolventDimethylformamideHCID 6228—
ProductHCID 59543587HCID 5954358751%

Reaction Steps

(2S,4R)-4-[4-(2,2,2-Trifluoro-ethoxy)-2-trifluoromethyl-benzenesulfonyl]-pyrrolidine-2-carboxylic acid (1-cyano-cyclopropyl)-amide (20 mg, 41 umol; example 211a) was dissolved in DMF (0.4 ml) under a N2-atmosphere at ambient temperature. 1-Trifluoromethyl-cyclopropanecarboxylic acid (10 mg, 62 umol; CAS Reg. No. 277756-46-4), HATU (23 mg, 62 umol) and DIEA (10 ul, 62 umol) were added and the reaction mixture was stirred for 48 h at ambient temperature. Ice water/brine 1/1 and iPrOAc were added and the layers were separated. The aqueous layer was extracted one more time with iPrOAc, the combined organic layers were washed with ice water/brine 1/1 and dried over Na2SO4. The solvent was removed under reduced pressure to give a yellow oil which was purified by preparative thin layer chromatography (silica gel, iPrOAc/heptane) to obtain the title compound (13 mg, 21 umol; 51%) as colorless solid. MS (ESI): m/z=622.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163793B2
Source datasetuspto-grants-2012_04
ORD IDord-8742c51a00d34805a730b5bdcd842f14
Source noteuspto-grants-2012_04