HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyloxyacetyl chloride → HCID 86620385, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyloxyacetyl chloride | HCID 177085 | — |
| Reactant | HCID 86620386 | HCID 86620386 | — |
| Product | HCID 86620385 | HCID 86620385 | — |
Reaction Steps
Using an analogous method to that described in Example 51, N-[5-(2-amino-4-methyl-1,3-thiazol-5-yl)-2-chloropyridin-3-yl]benzenesulfonamide was reacted with 2-benzyloxyacetyl chloride. The reaction product was purified by preparative HPLC (Method A) to give the title product (retention time 9.6 minutes); 1H NMR Spectrum: (DMSOd6+D2O) 8.56 (1H, d); 8.09 (1H, d); 8.03 (2H, br d); 7.83 (1H, t); 7.70 (2H, t); 7.31-7.26 (3H); 7.26-7.24 (2H); 4.41 (2H, AB system); 4.12 (1H, d); 3.86 (1H, d); 2.24 (3H, s); Mass Spectrum: M+H+ 529.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07868188B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-25b3735ca41246568ef6f512e55650af |
| Source note | uspto-grants-2011_01 |