HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine tetrahydrofuran → 4-(Methyaminomethyl)phenyloxycarbonyl-glutamic acid di-tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine tetrahydrofuran | HCID 66615946 | — |
| Reactant | 4-Formylphenyloxycarbonyl-glutamic acid di-tert-butyl ester | HCID 87930423 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Methyaminomethyl)phenyloxycarbonyl-glutamic acid di-tert-butyl ester | HCID 69644845 | 78% |
Reaction Steps
A stirred solution of 40 (6.1 g, 14.9 mmol) in dichloromethane (50 mL) was treated with 2 N methylamine-THF solution (10 mL) at 0° C. overnight. After removal of solvents, the residual oil was dissolved in methanol (80 mL) and placed in an ice-bath. To the above solution was added sodium borohydride in small portions over 30 min. The reaction solution was kept at 0° C. for 1 hour, and solvent was then evaporated. The residue was worked up with brine and dichloromethane. After separation, the organic phase was dried over anhydrous MgSO4, rotary evaporated and dried in vacuum. The crude amine 41 (5.4 g, 78%) was obtained as a light yellow glassy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06855695B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-581076baa3bd49d7840e6c654d9bdd43 |
| Source note | uspto-grants-2005_02 |