HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → tert-Butyl (1(S)-(2-azido-1(S)-hydroxyethyl)-3(S)-{[2-(3-methoxypropoxy)benzoylamino]-methyl}4-methylpentyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | tert-butyl (3(S)-{[2-(3-methoxypropoxy)benzoylamino]methyl}-4-methyl-1(S)-(R)-oxiranylpentyl)-carbamate | HCID 86613450 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | tert-Butyl (1(S)-(2-azido-1(S)-hydroxyethyl)-3(S)-{[2-(3-methoxypropoxy)benzoylamino]-methyl}4-methylpentyl)carbamate | HCID 86613457 | — |
Reaction Steps
The solution of 0.600 g of tert-butyl (3(S)-{[2-(3-methoxypropoxy)benzoylamino]methyl}-4-methyl-1(S)—(R)-oxiranylpentyl)carbamate (Example 1b) in 12 ml of methanol is admixed with 0.208 g of sodium azide and 0.123 g of ammonium chloride, and stirred at reflux over 6 hours. The reaction solution is cooled, poured onto ice-water and extracted with tert-butyl methyl ether (2×). The combined organic phases are washed with water and brine, dried over sodium sulphate and concentrated by evaporation. The title compound is obtained from the residue by means of flash chromatography (SiO2 60F) as a colourless oil. Rf=0.37 (2:1 EtOAc-heptane); Rt=18.95 (gradient II).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07786307B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-b0666a9316da45f09d37424ea70ca055 |
| Source note | uspto-grants-2010_08 |