HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 4-(Acetyl-cyclopropyl-amino)-piperidine-1-carboxylic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-Butyl 4-(cyclopropylamino)piperidine-1-carboxylate | HCID 2769591 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Acetyl-cyclopropyl-amino)-piperidine-1-carboxylic acid tert-butyl ester | HCID 68772516 | — |
Reaction Steps
To a solution of 4-cyclopropylamino-piperidine-1-carboxylic acid tert-butyl ester (1.0 g, 4.2 mmol) in DCM (22 mL) was added DIEA (0.8 mL, 4.6 mmol) and acetic anhydride (0.42 mL, 4.4 mmol). The mixture was stirred (rt, 16 h). After washing the solution with 1 N NaOH and brine, the organic layer was dried and concentrated to an orange oil (1.15 g, 98%). MS (ESI): mass calcd. for C15H26N2O3, 282.19; m/z found, 283.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399465B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-9b7014b6dd8341e88cd311bec1b2a3b3 |
| Source note | uspto-grants-2013_03 |