HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 68544240, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | HCID 68548829 | HCID 68548829 | — |
| Product | HCID 68544240 | HCID 68544240 | 58% |
Reaction Steps
Step B Amide Formation: Addition of acetyl chloride (0.05 mL, 0.65 mmol) to 7-(Cyclohexylmethyl-amino)-1-ethoxycarbonylmethoxy-3,8-dithia-cyclopenta[a]indene-2-carboxylic acid methyl ester (60 mg, 0.13 mmol) was carried out following a procedure similar to that delineated in Step B, Example 27, affording 38 mg of 7-(Acetyl-cyclohexylmethyl-amino)-1-ethoxycarbonylmethoxy-3,8-dithia-cyclopenta[a]indene-2-carboxylic acid methyl ester as a yellow solid. (58% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07674822B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-f6a135775aba411a80bb0f92ae81d95f |
| Source note | uspto-grants-2010_03 |