Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 57713927 | HCID 57713927 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl acetate hexane | HCID 21226206 | 72% |
Reaction Steps
4-(Methylamino)-3-(morpholinosulfonyl)benzoyl chloride (1.4.Aa, 100 mg, 1.5 eq) was dissolved in 8 mL of dry dichloromethane. Next, S-fenchyl amine (prepared as reported in FR96/01953) (Bb, 0.032 mL, 1 eq) was added. Triethylamine (0.030 mL, 1 eq) was then added. The progress of the reaction was monitored by TLC in 85% ethyl acetate:hexane. After 45 minutes the product was washed with H2O, 1.0 M HCl, and brine. The dichloromethane was evaporated and crystals were obtained. The crude product 1A was purified on a silica gel column using hexane/ethyl acetate [66 mg of purified product was obtained (72% yield)]. MS analysis (m+1)=436.6. 1H NMR (CDCl3), δ 0.84 (s, 3H), 1.10 (s, 3H), 1.18 (s, 3H), 1.26 (m, 3H), 1.51 (m, 1H), 1.61 (s, 2H), 1.72 (d, 2H), 1.81 (m, 1H), 2.91 (d, J=5 Hz, 3H), 3.08 (t, J=5 Hz, 4H), 3.72 (t, J=5 Hz, 4H), 3.81 (dd, J=9 Hz and 2 Hz, 1H), 5.93 (d, J=9 Hz, 1H), 6.63 (d, J=5 Hz, 1H), 6.75 (d, J=9 Hz, 1H), 7.83 (q, J=8 Hz and 2 Hz, 1H), 8.02 (d, J=2 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07544676B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-54f643614a5c4ac682e790e16bd71c28 |
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| Source note | uspto-grants-2009_06 |
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