Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 13969852 | HCID 13969852 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131723255 | HCID 131723255 | 92% |
Reaction Steps
The product from (A) (3.8 mmol) was dissolved in dimethylformamide (DMF) (20 mL) and the solution was cooled to 0° C. Methanesulfonyl chloride (14.4 mmol) and triethylamine At3N) (14.4 mmol) were added. The reaction was stirred at 0° C. for 2 hr, quenched with H2O (2×25 mL), saturated NaHCO3 (1×25 mL) and brine (1×25 mL). The organic layer was dried over Na2SO4, filtered and dried to give the title compound (1.2g, 92%) as a white solid: 1H NMR (400 MHz, CDCl3) δ 1.60 (9H, s), 1.91-2.05 (2H, m), 2.77-2.90 (2H, m), 3.68-3.82, 3.12 (3H, s), 3.9-4.05 (1H, m), 4.27-4.4 (2H, m), 4.72-4.82 (1H, m), 7.25-7.48 (5H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06399629B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-d02c540230b44c16a31d2c48a71185e9 |
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| Source note | uspto-grants-2002_06 |
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