HuagongsheHuagongshe Chemistry Print Report · For research reference only
Citric Acid → HCID 67507507, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Bromomethyl)benzonitrile | HCID 86996 | — |
| Reactant | HCID 67507232 | HCID 67507232 | — |
| Reactant | HCID 67507766 | HCID 67507766 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67507507 | HCID 67507507 | 84.3% |
Reaction Steps
3-[(2S,4S)-1-tert-Butoxycarbonyl-4-(4-cyanophenylsulfonyl)amino-2-pyrrolidinylcarbonyl]-1,3-thiazolidine [product of Example 123 (1), 856 mg] was dissolved in DMF (20 mL), and potassium carbonate (380 mg) and 4-cyanobenzyl bromide (400 mg) were added thereto at room temperature. The mixture was stirred for 4 hr. To the reaction mixture was added 10% citric acid solution, and the precipitate was collected by filtration to give 3-{(2S,4S)-1-tert-butoxycarbonyl-4-[N-(4-cyanophenylmethyl)-N-(4-cyanophenylsulfonyl)amino]-2-pyrrolidinylcarbonyl}-1,3-thiazolidine (900 mg) as a pale-yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07074794B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-d78402d1c48e463d8efe9e734f7ec81b |
| Source note | uspto-grants-2006_07 |