HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloromethylnaphthalene → N-(4-Chlorophenyl)-N'-{[4-(1 naphthylmethyl)morpholin-2-yl]methyl}urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloromethylnaphthalene | HCID 6845 | — |
| Reactant | N-(4-Chlorophenyl)-N'-(morpholin-2-ylmethyl)urea | HCID 23089254 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(4-Chlorophenyl)-N'-{[4-(1 naphthylmethyl)morpholin-2-yl]methyl}urea | HCID 17984726 | — |
Reaction Steps
To a stirred solution of Intermediate 9 (0.01 g) in N,N-dimethylformamide (1 ml) was added 1-(chloromethyl)naphthalene (6.1 μl). The mixture was stirred at 22° C. for 24 h before tris-(2-aminoethyl)amine polystyrene (Argonaut Technologies, 0.01 g @ 4.46 mmol/g) and polystyrene methyl isocyanate (Argonaut Technologies, 0.033 g @ 1.39 mmol/g) was added. Stirring was continued for a further 2 h before the mixture was purified by solid phase extraction (Isolute SCX sulphonic acid column), eluting with methanol followed by 10% 0.880 ammonia solution in methanol. The basic fraction was evaporated in vacuo to give the title compound (0.003 g). LC/MS (System A) Rt 2.82 min, Mass Spectrum m/z 4140 [MH+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157457B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-4972870b008c4989915a16eccce2a1f7 |
| Source note | uspto-grants-2007_01 |