Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 58001277 | HCID 58001277 | — |
| Product | HCID 87393674 | HCID 87393674 | 65% |
Reaction Steps
Under ice cooling, 2-aminothiazole (65 mg, 0.64 mmol) was added to a solution of N,N′-carbonyldiimidazole (110 mg, 0.68 mmol) in THF (3.0 mL), and then the reaction mixture was stirred for 6 hours. N-(2-t-butoxycarbonylaminophenyl)-4-[3-(morpholin-4-yl) propylaminomethyl]benzamide (Reference Compound No. 4-11, 110 mg, 0.23 mmol) was added thereto, and then the reaction mixture was stirred at 60° C. for 16 hours. Water (100 mL) was added thereto, the whole was extracted with ethyl acetate (100 mL), and then the organic layer was washed with brine (100 mL). The organic layer was dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (chloroform-methanol) to give 90 mg of the title reference compound as a colorless amorphous product. (Yield 65%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076332B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-7998306f4a37444fa44e0e3e8ac5396f |
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| Source note | uspto-grants-2011_12 |
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