HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42551Generated: October 30, 2026
Triethylamine → HCID 59475009, compound
https://huagongshe.com/reaction/42551
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | (S)-4-(4-chlorophenyl)-3,3-dimethylpiperidin-4-ol | HCID 18437142 | — |
| Reactant | (1R,2S)-2-{[(tert-butoxy)carbonyl]amino}cyclobutane-1-carboxylic acid | HCID 68495906 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59475009 | HCID 59475009 | 96.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08536198B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-08f1dd65681040e4a09cb0d057b36abd |
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| Source note | uspto-grants-2013_09 |
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