Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl isocyanate | HCID 76639 | — |
| Reactant | [4-(3,4-Dichlorobenzyl)morpholin-2-yl]methylamine | HCID 10308229 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10294861 | HCID 10294861 | — |
Reaction Steps
To a stirred solution of Intermediate 3 (0.025 g) in dichloromethane (1 ml) was added benzylisocyanate (16.8 pt). The mixture was stirred at 22° C. for 18 h before tris-(2-aminoethyl)amine polystyrene (Argonaut Technologies, 0.04 g @ 3.85 mmol/g) was added. Stirring was continued for a further 72 h before the mixture was poured onto a 1 g solid phase extraction (Isolute SCX sulphonic acid) cartridge. The cartridge was washed with methanol before eluting with 10% 0.880 ammonia solution in methanol. The basic fraction was evaporated in vacuo to give a pale yellow solid. The solid was purified by eluting through a 1 g silica solid phase extraction cartridge (Varian Bondelut) eluting sequentially with dichloromethane, ether, ethyl acetate, acetone, acetonitrile and methanol, to give the title compound as a white solid (0.031 g). LC/MS (System A) Rt 2.22 min, Mass Spectrum m/z 408 [MH+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157457B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-e6240a7227e04959ba571b2ed1ce73f6 |
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| Source note | uspto-grants-2007_01 |
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