HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Ammonium Hydroxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 67390064 | HCID 67390064 | — |
| Product | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 131730921 | HCID 131730921 | — |
Reaction Steps
A solution of (±)-5-{[(benzyloxy)carbonyl]amino)-2-tert-butoxycarbonyl)amino]indane-2-carboxylic acid from Step B (829 mg, 1.94 mmol), ammonium chloride (208 mg, 3.89 mmol), pyBOP (1.52 g, 2.92 mmol), and DIEA (1.35 mL, 7.78 mmol) in DMF (3 mL) was stirred at ambient temperature for 16 h. The reaction mixture was poured onto saturated NaHCO3 (20 mL) and extracted with CH2Cl2 (3×20 mL). The combined organic layers were dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude product was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:MeOH:NH4OH—100:0:0 to 90:9:1, to give the title compound, MS: m/z=426 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08569291B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-f8b27d2c18d34d87b55629c9d5cc563a |
| Source note | uspto-grants-2013_10 |