HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-4-chlorobenzenethiol → N-{4-[({2-[(1-benzofuran-2-ylsulfonyl)amino]-4-chlorophenyl}thio)methyl]-1,3-thiazol-2-yl}acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-4-chlorobenzenethiol | HCID 12000 | — |
| Reactant | 2-Acetamido-4-chloromethylthiazole | HCID 81963 | — |
| Reactant | 1-Benzofuran-2-sulfonyl chloride | HCID 2795172 | — |
| Product | N-{4-[({2-[(1-benzofuran-2-ylsulfonyl)amino]-4-chlorophenyl}thio)methyl]-1,3-thiazol-2-yl}acetamide | HCID 86667126 | — |
Reaction Steps
Following General Procedure A, B, the title compound was prepared from 2-amino-4-chloro-benzenethiol, N-(4-Chloromethyl-thiazol-2-yl)-acetamide and 1-benzofuran-2-sulfonyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877804B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-7fd66d42027542fe952c3531c60c30a0 |
| Source note | uspto-grants-2014_11 |