HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → Methyl 1-(2-fluorophenyl)-5-(morpholin-4-ylmethyl)-1H-1,2,3-triazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Methyl 4-chloroacetoacetate | HCID 36240 | — |
| Reactant | 1-Azido-2-fluorobenzene | HCID 11607924 | — |
| Product | Methyl 1-(2-fluorophenyl)-5-(morpholin-4-ylmethyl)-1H-1,2,3-triazole-4-carboxylate | HCID 68649638 | — |
Reaction Steps
A solution of 1-azido-2-fluorobenzene, prepared according to Platz, M. S. et al. J. Org. Chem. 1989, 54, 5938-5945 (500 mg; 3.65 mmol; 1 eq.) and methyl 4-chloroacetoacetate (823 mg; 5.47 mmol; 1.5 eq.) in morpholine (10 ml) was stirred at 50° C. overnight. The reaction mixture was evaporated. Water was added (20 mL) and was extracted with EtOAc (2×20 mL). Combined organic phases were extracted with 3 portions of HCl 1 N. Combined aqueous phases were made alkaline with NaOH 5N and were extracted with EtOAc (3×20 mL). Organic layers were dried over magnesium sulfate and evaporated, affording the title product as a dark red oil. It was used in the next step without further purification. HPLC (Method A) Rt 1.81 min. (Purity: 82.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08202856B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-d420a75a5add4873a536843d43ff921c |
| Source note | uspto-grants-2012_06 |