Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42551Generated: October 30, 2026

Triethylamine → HCID 59475009, compound

https://huagongshe.com/reaction/42551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant(S)-4-(4-chlorophenyl)-3,3-dimethylpiperidin-4-olHCID 18437142—
Reactant(1R,2S)-2-{[(tert-butoxy)carbonyl]amino}cyclobutane-1-carboxylic acidHCID 68495906—
SolventDichloromethaneHCID 6344—
ProductHCID 59475009HCID 5947500996.1%

Reaction Steps

A mixture of (S)-4-(4-chlorophenyl)-3,3-dimethylpiperidin-4-ol (91 mg, 0.381 mmol), (±)-(cis)-2-(tert-butoxycarbonylamino)cyclobutanecarboxylic acid (82 mg, 0.381 mmol), and triethylamine (0.186 mL, 1.333 mmol) in methylene chloride (5 mL) was treated with BOP (168 mg, 0.381 mmol), and the mixture was stirred overnight at room temperature. At the conclusion of this period, the solvent was evaporated with a stream of nitrogen, and the resulting residue was taken up in ethyl acetate. The resulting mixture was washed 3× with saturated sodium carbonate, 3× with 1 N HCl, once with water, and once with brine, then the organic phase was concentrated in vacuo to yield the title compound (160 mg, 96% yield) as a colorless glass. The material was used as-is without further purification. MS (ESI+)=437.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536198B2
Source datasetuspto-grants-2013_09
ORD IDord-08f1dd65681040e4a09cb0d057b36abd
Source noteuspto-grants-2013_09