HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 4-Benzyloxybenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Benzyloxybenzoylchloride | HCID 3766410 | — |
| Product | 4-Benzyloxybenzamide | HCID 2726431 | — |
Reaction Steps
A solution of 3R-carboxylate-6-nitro-2H-3,4-dihydro-[2-1b]imidazopyran (Example 21, 1 eq.), triethylamine (1 eq.), diphenylphosphoryl azide (1 eq.) in toluene is heated at 80° C. for 4 h, cooled and t-butanol is added. The reaction is warmed to 70° C. for an additional 1 h. Workup in the standard fashion gives the Boc amine. Deprotection of the Boc group (trifluoroacetic acid:dichloromethane, 1:1) and addition of 4-benzyloxybenzoyl chloride and triethylamine gives the 4-benzyloxybenzamide of 3R-amino-6-nitro-2H-3,4-dihydro-[2-1b]imidazopyran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06087358 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-9a395a53875342bea4d103d19cd2f2e7 |
| Source note | uspto-grants-2000_07 |