Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 5-Mesyl-o-anisic acid | HCID 170840 | — |
| Reactant | 1,2-Diethyl-4-pyrazolidinamine | HCID 559199 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13746892 | HCID 13746892 | 109.7% |
Reaction Steps
Triethylamine (1.01 g, 0.010 mole) was added to a stirred mixture of 5-methylsulfonyl-2-methoxybenzoic acid (2.30 g, 0.010 mole) in 50 ml of methylene chloride. The mixture was cooled to 0° C. for 20 minutes and maintained at this temperature while ethyl chloroformate (1.09 g, 0.010 mole) was added dropwise. After another 20 minutes of stirring at 0° C., a solution of 1,2-diethyl-4-aminopyrazolidine (2.43 g, 0.010 mole) in 10 l of methylene chloride was added dropwise. The reaction mixture was allowed to come to ambient temperature and was stirred for 18 hrs. The reaction mixture was then extracted with 10% sodium bicarbonate solution, the methylene chloride layer separated and dried over magnesium sulfate. The methylene chloride solution was concentrated to give 3.90 g of a tanbrown solid which was recrystallized from water. A sulfate salt was prepared which was converted back to the free base. The solid free base that formed was recrystallized from ethanol-isopropyl ether to give 1.03 g (29%) of title compound; m.p. 123°-124° C. The compound was vacuum dried at 110° C.; the melting point was unchanged.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04624961 |
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| Source dataset | uspto-grants-1986_11 |
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| ORD ID | ord-2c93560398f644b29a6abdb95ff1479e |
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| Source note | uspto-grants-1986_11 |
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