Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 2,6-Dichlorobenzyl chloride | HCID 74832 | — |
| Reactant | HCID 178419078 | HCID 178419078 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53929760 | HCID 53929760 | 56.5% |
Reaction Steps
L-histidine (3.13 g) was added to a solution of NaNH2 in liquid ammonia prepared from Na (0.93 g) and FeCl3 (catalytic amount) in liquid ammonia (50 ml) After 15 min., a solution of 2,6-dichlorobenzylchloride (3.96 g) in THF (5 ml) was added and the mixture was stirred for 3 hr. The reaction mixture was quenched with H2O and ether. The pH of the aqueous layer was adjusted to pH 8 with 5% HCl followed by cooling. The resulting precipitate was collected by filtration, washed with H2O, and dried to give 1-[(2,6-dichlorophenyl)methyl]-L-histidine (3.58 g). The obtained compound (0.80 g) was dissolved in MeOH (30 ml) and HCl gas was bubbled for 10 min. at 0° C. The reaction mixture was stirred for 15 hr. at room temperature and the solvent was removed in vacuo to give 1-[(2,6-Dichlorophenyl)methyl]-L-histidine methyl ester, dihydrochloride salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06482849B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-288d6c3ab9624c1d80482818a56a1b93 |
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| Source note | uspto-grants-2002_11 |
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