HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 12642259, compound → HCID 178440131, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 12642259 | HCID 12642259 | — |
| Reactant | HCID 178441731 | HCID 178441731 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178440131 | HCID 178440131 | — |
Reaction Steps
Under nitrogen, a solution of 18.9 g (100 mmol) of N-Boc glycine hydrazide (from step 2 of Example 3) in 100 mL of methanol is treated with 11.5 g (100 mmol) of ethyl iminobutyrate [P. Reynaud and R. C. Moreau, Bull. Soc. Chim. France, 2997 (1964)]. The reaction is stirred at reflux overnight and concentrated in vacuo. Purification by silica gel chromatography (Waters Prep-500A) gives 5-propyl-3-tert-butoxycarbonylaminomethyl-1H-1,2,4-triazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132437B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-e70a072439d94f21b45873661df60afb |
| Source note | uspto-grants-2006_11 |