HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Chlorothiophene-2-carbonyl Chloride → tert. Butyl 3-[(5-chloro-thiophene-2-carbonyl)-amino]-pyrrolidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Chlorothiophene-2-carbonyl Chloride | HCID 589223 | — |
| Reactant | 1-Boc-3-aminopyrrolidine | HCID 2756370 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert. Butyl 3-[(5-chloro-thiophene-2-carbonyl)-amino]-pyrrolidine-1-carboxylate | HCID 68646970 | — |
Reaction Steps
0.5 g (2.7 mmol) tert. Butyl 3-amino-pyrrolidine-1-carboxylate are dissolved in 7 ml DCM, combined with 1.4 ml (10.1 mmol) TEA and 0.5 g (2.7 mmol) 5-chloro-thiophene-2-carboxylic acid chloride and stirred for one hour at RT. The reaction mixture is diluted with DCM and washed successively with dil. aqueous KHSO4 solution, sat. aqueous NaHCO3 solution and water. The combined organic phases are dried on sodium sulphate and evaporated to dryness i. vac.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08309542B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-c32fbf20bda846a49cf2ae3ac3baa02f |
| Source note | uspto-grants-2012_11 |