HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 15614790, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chloromethyl pivalate | HCID 87885 | — |
| Reactant | CCK antagonist synthetic 20 | HCID 14208232 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15614790 | HCID 15614790 | — |
Reaction Steps
A mixture of 1-carboxymethyl-1,3-dihydro-3-(2-indolecarbonylamino)-5-phenyl-2H-1,4-benzodiazepin-2-one (85 mg, 0.20 mmol), pivaloyloxymethylchloride (32 μl, 0.22 mmol) and triethylamine (28 μl, 0.20 mmol) was combined in 2 ml of dry dimethylformamide and allowed to stand at room temperature for 48 hours. Solvent was removed under reduced pressure and the residue partitioned between ethyl acetate and water. Extractive work-up gave 100 mg of crude Product which was chromatographed on silica gel (CH3OH-CHCl3, 3:97 v/v elution) to give a white solid after trituration with ether: m.p. 225°-226° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04820834 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-79688120b4b14035909201a7143eed02 |
| Source note | uspto-grants-1989_04 |