HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonamide → HCID 76169163, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | HCID 74058496 | HCID 74058496 | — |
| Product | HCID 76169163 | HCID 76169163 | 67% |
Reaction Steps
Reaction of 4-({[2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetyl]-methoxy-amino}-methyl)-benzoic acid tert-butyl ester (0.060 g, 0.15 mmol) with methanesulfonamide (0.014 g, 0.15 mmol) as described in the prepartion of compound 22 gave 0.043 g (67% yield) of the title amide as a white solid. 1H NMR (400 MHz, CDCl3) δ: mixture of rotamers: 1.58 (9H, s t-Bu), 3.31, 3.33 and 3.36 (3H, 3 S, SO2CH3), 3.61, 3.66 and 3.70 (3H, 3 s, OCH3), 4.8 and 4.88 (2H, 2 s, NCH2), 6.6 (1H, s, CH), 7.28 (2H, m, aromatics), 7.98 (2H, m, aromatics), 8.98 (1H, broad s, NH). HRMS (ESI/neg) calculated for C18H23N2O8S: [M−H]−: 427.117513; found: 427.117342.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06890942B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-5fdf9f81837a463dac6ea354450160be |
| Source note | uspto-grants-2005_05 |