HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466003Generated: November 1, 2026
Water → 3-Carbamoylisoxazol-5-ylmethyl (-)-(R)-3-(naphth-2-yloxymethyl)pyrrolidine-1-carboxylate
https://huagongshe.com/reaction/1466003
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | (R)-3-(naphth-2-yloxymethyl)pyrrolidine | HCID 26192527 | — |
| Reactant | 3-Carbamoylisoxazol-5-ylmethyl 4-nitrophenyl carbonate | HCID 66660860 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Carbamoylisoxazol-5-ylmethyl (-)-(R)-3-(naphth-2-yloxymethyl)pyrrolidine-1-carboxylate | HCID 67350914 | 38.5% |
Reaction Steps
0.21 g (0.92 mmol) of (R)-3-(naphth-2-yloxymethyl)-pyrrolidine is dissolved in 3.80 ml of dichloromethane and then 0.31 g (1.01 mmol) of 3-carbamoylisoxazol-5-ylmethyl 4-nitrophenyl carbonate and 0.15 ml (1.38 mmol) of N-methylmorpholine are added. The mixture is stirred at ambient temperature for 20 hours and then water is added to the reaction medium. After extraction of the aqueous phase with dichloromethane, the organic phases are successively washed three times with a 1M aqueous sodium hydroxide solution and then twice with a saturated aqueous ammonium chloride solution. After having dried the organic phases over sodium sulphate, they are filtered and the filtrate is evaporated to dryness. 0.14 g of the desired product is thus obtained in the form of a white solid after purification on a column of silica gel, elution being carried out with a dichloromethane/methanol mixture, and then taken up in isopropyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09000010B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-a9c4d1cdfe134fa2be194f04004afc87 |
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| Source note | uspto-grants-2015_04 |
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