HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 86587153, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 10295709 | HCID 10295709 | — |
| Product | HCID 86587153 | HCID 86587153 | — |
Reaction Steps
A mixture of 2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-(2-ethoxycarbonyl-2-oxo-ethylsulfanyl)-ethylcarbamoyl]-butyric acid (200 mg) and p-toluenesulfonic acid (30 mg) in methanol (100 mL) was heated to reflux for 72 h. The solvent was then evaporated and the residue was dried under high vacuum to afford the desired product, 2-amino-4-[2-(2-ethoxycarbonyl-2-oxo-ethylsulfanyl)-1-(methoxycarbonylmethyl-carbamoyl)-ethylcarbamoyl]-butyric acid methyl ester, as a yellowish sticky solid. 1H-NMR (D3COD, 300 MHz) δ (ppm): 6.24 (d, J=10.5 Hz, 0.22 H), 4.49-4.4.33 (m, 1H), 4.15-3.91 (m, 3H), 3.76 (s, 3H), 3.65-3.57 (m, 2H), 3.51 (s, 3H), 3.21-2.73 (m, 2.8 H), 2.45-2.43 (m, 2H), 2.10-1.92 (m, 2H), 1.13-1.03 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06900218B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-5204274b5176428f8cae7b4613c3ddaf |
| Source note | uspto-grants-2005_05 |