HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 69584372, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 2,6-Dimethyl-benzoic acid 3-amino-4-tert-butoxycarbonyl-2-oxo-butyl ester | HCID 23571411 | — |
| Reactant | HCID 69584313 | HCID 69584313 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69584372 | HCID 69584372 | — |
Reaction Steps
To a solution of 6-[(naphthalene-2-carbonyl)-amino]-5-oxo-1,2,3,5,6,7,10,10a-octahydro-pyrrolo[1,2-a]azocine-3-carboxylic acid, (124 mg, 0.33 mmol)in dichloromethane is added EDCI (191 mg, 1 mmol), 2,6-dimethyl-benzoic acid 3-amino-4-tert-butoxycarbonyl-2-oxo-butyl ester, 111, (200 mg, 0.62 mmol), and triethylamine (150 ul). After consumption of the starting material, the reaction is washed with 1N HCl (1×50 ml), water (1×50 ml), and brine (1×50 ml). The CHCl2 is reduced in vacuo. The residue is used directly in the next step without purification. ESI MS 696.1 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07041696B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-fec5b9e3aa1d47a79127774db1d5d37f |
| Source note | uspto-grants-2006_05 |