HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 14809494, compound → HCID 20143011, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 14809494 | HCID 14809494 | — |
| Reactant | HCID 20143023 | HCID 20143023 | — |
| Reactant | HCID 86742111 | HCID 86742111 | — |
| Product | HCID 20143011 | HCID 20143011 | 72% |
| Product | HCID 20143097 | HCID 20143097 | 12.8% |
| Product | HCID 20143168 | HCID 20143168 | 64.9% |
Reaction Steps
3,4-Dihydro-2-(2-hydroxy-5-methoxyphenyl)-4-methyl-2-methylthio-3-oxo-2H-1,4-benzothiazine (5.2 g, compound No. 8), β-chloropropionaldehyde diethyl acetate (3.0 g) and N-methyl-2-(3,4-dimethoxyphenyl)propylamine hydrochloride (5.2 g) are treated by the similar method as in Example 26 to give 4.7 g (64.9%) of 2-[2-(3,3-diethoxypropoxy)-5-methoxyphenyl]-3,4-dihydro-4-methyl-2-methylthio-3-oxo-2H-1,4-benzothiazine (compound No. 21, (IR: neat, cm-1) 1660, 1555, 1048, 750), 2.8 g (72.0%) of 3,4-dihydro-2-[5-methoxy-2-(3-oxopropoxy)phenyl]-4-methyl-2-methylthio-3-oxo-2H-1,4-benzothiazine (compound No. 22, (IR: neat, cm-1) 1722, 1658, 1588, 1036, 748) and 0.6 g (12.8%) of the titled compound (mp. 153°-156.5° C. (dec.)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04739050 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-29f48d8f315246dc918b6e4e7ecb102d |
| Source note | uspto-grants-1988_04 |