HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → methyl 5-{2-[((2S)-2-{[(benzyloxy)carbonyl]amino}-3-bromopropyl)oxy]phenyl}-6-cyclohexyl-3-methyl-4H-thieno[3,2-b]pyrrole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Methyl 5-{2-[((2R)-2-{[(benzyloxy)carbonyl]amino}-3-hydroxypropyl)oxy]phenyl}-6-cyclohexyl-3-methyl-4H-thieno[3,2-b]pyrrole-2-carboxylate | HCID 67298563 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | methyl 5-{2-[((2S)-2-{[(benzyloxy)carbonyl]amino}-3-bromopropyl)oxy]phenyl}-6-cyclohexyl-3-methyl-4H-thieno[3,2-b]pyrrole-2-carboxylate | HCID 67298840 | 86% |
Reaction Steps
Methyl 5-{2-[((2R)-2-{[(benzyloxy)carbonyl]amino}-3-hydroxypropyl)oxy]phenyl}-6-cyclohexyl-3-methyl-4H-thieno[3,2-b]pyrrole-2-carboxylate and triphenylphosphine (2.27 eq.) were dissolved in DCM (0.02M) and K2CO3 (4.31 eq.) was added. To the stirred mixture CBr4 (2.22 eq.) was added and the yellowish reaction mixture was left stirring at RT for 3 h. All volatiles were evaporated i. vac. and the residual material was subjected to chromatography (PE:EtOAc, 8.5:1.5). The product was obtained as a yellowish sticky solid (86%). MS (ES+) m/z 639, 641 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07973026B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-68963da2782f43bd96a4ad4716e506ea |
| Source note | uspto-grants-2011_07 |