HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 68415475, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 68414384 | HCID 68414384 | — |
| Product | HCID 68415475 | HCID 68415475 | — |
Reaction Steps
A solution of 3.66 g of [3-(4-amino-1H-benzoimidazol-2-yl)-propyl]-methyl-carbamic acid tert-butyl ester in 40 mL of acetic anhydride was refluxed for 2 h. The excess of acetic anhydride was evaporated off and the residue was treated with 16 mL of EtOH and IM-NaOH until pH 10 then extracted with EtOAc. The organic phase was dried over anh. Na2SO4 and concentrated in vacuo. Purification by CC using EtOAc/MeOH 100/1 to 90/1 yielded 1.86 g of [3-(4-acetylamino-1H-benzoimidazol-2-yl)-propyl]-methyl-carbamic acid tert-butyl ester as yellow foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08202885B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-0ae2e56943aa4ad9929c67571ab01696 |
| Source note | uspto-grants-2012_06 |