HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876725Generated: October 30, 2026
1,1'-Carbonyldiimidazole → HCID 86762757, compound
https://huagongshe.com/reaction/876725
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Benzoyl isothiocyanate | HCID 68284 | — |
| Reactant | [(3R,4S)-1-allyl-4-amino-4-(3-bromophenyl)pyrrolidin-3-yl]methanol | HCID 86762758 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86762757 | HCID 86762757 | 68.2% |
Reaction Steps
A solution of [(3R,4S)-1-allyl-4-amino-4-(3-bromophenyl)pyrrolidin-3-yl]methanol (27 g; 86.7 mmol) in tetrahydrofuran (270 mL) is cooled to −5° C. under a nitrogen atmosphere. Benzoyl isothiocyanate (12.3 mL, 91 mmol) is added drop wise keeping the temperature below 0° C. The reaction is allowed to warm to 22° C. over 1 hour. 1,1′-Carbonyldiimidazole (28.1 g, 173.5 mmol) is added in a single portion and the reaction is stirred for 1 hour at 22° C. and then heated to reflux for 16 hours. The solvent is removed in vacuo and the residue dried under vacuum. The crude material is partitioned in methyl tert-butyl ether (500 mL) and water (250 mL). The organic layer is separated, dried over magnesium sulfate, filtered and evaporated to dryness. The crude material is purified over a silica gel gradient of 90/10 to 60/40 methylene chloride/ethyl acetate to give the title compound (27 g, 68%). ES/MS (m/e): 456 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08987254B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-e5ff4a2e3064472394dfec7e3243e5a9 |
|---|
| Source note | uspto-grants-2015_03 |
|---|