HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 67023487, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | HCID 17756583 | HCID 17756583 | — |
| Reactant | HCID 67023499 | HCID 67023499 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 67023487 | HCID 67023487 | — |
Reaction Steps
To a stirred solution of 4-tert-butoxycarbonylamino-4-(S)-cyclohexyl-butyric acid (2.63 g, 9.2 mmole) were added (1-benzyl-1H-tetrazol-5-ylmethyl)-cyclohexyl-amine (2.50 g, 9.2 mmole) and N,N-diisopropylethylamine (3.2 mL, 18.4 mmole) in DMF (50 mL) and HBTU (4.19 g, 11.0 mmole). After stirring at room temperature overnight, the reaction mixture was diluted with diethyl ether (200 mL). The reaction mixture was extracted with water three times and dried over magnesium sulfate. The solution was concentrated to yield {3-[(1-benzyl-1H-tetrazol-5-ylmethyl)-cyclohexyl-carbamoyl]-(S)-cyclohexyl-propyl}-carbamic acid as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531545B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-4a46719d6f0e4542a2e6f387a8a922ad |
| Source note | uspto-grants-2009_05 |