HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium diisopropylamide → (2R,4S)-N-allyloxycarbonyl-2-[(5S)-5-hydroxymethyl-2-oxopyrrolidin-3-ylmethyl]-4-tritylthiopyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | N-tert-butyldimethylsilyl-5-tert-butyldimethylsiloxymethyl-2-oxopyrrolidine | HCID 57036326 | — |
| Reactant | (2S,4S)-N-allyloxycarbonyl-2-iodomethyl-4-tritylthiopyrrolidine | HCID 57112975 | — |
| Product | (2R,4S)-N-allyloxycarbonyl-2-[(5S)-5-hydroxymethyl-2-oxopyrrolidin-3-ylmethyl]-4-tritylthiopyrrolidine | HCID 57189868 | 21% |
Reaction Steps
The same procedure as in Reference Example 22-1 was carried out by using N-tert-butyldimethylsilyl-5-tert-butyldimethylsiloxymethyl-2-oxopyrrolidine (10.67 g, 31.6 mmol), lithium diisopropylamide (2.1M tetrahydrofuran solution, 15.1 ml, 31.6 mmol) and (2S,4S)-N-allyloxycarbonyl-2-iodomethyl-4-tritylthiopyrrolidine (10 g, 17.6 mmol) to obtain (2R,4S)-N-allyloxycarbonyl-2-[(5S)-5-hydroxymethyl-2-oxopyrrolidin-3-ylmethyl]-4-tritylthiopyrrolidine (2 g, yield: 21%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05374720 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-ff67efe4b82f4f33816effd65cff8a64 |
| Source note | uspto-grants-1994_12 |