HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 69589137, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Ethyl isocyanatoacetate | HCID 76283 | — |
| Reactant | HCID 69545433 | HCID 69545433 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69589137 | HCID 69589137 | — |
Reaction Steps
A solution of 5-amino-3-[1-(pyrrol-2-yl)ethylidene]indolin-2-one (360 mg, 1.5 mmol) in tetrahydrofuran (15 mL) was treated with ethyl isocyanatoacetate (195 mg, 1.5 mmol) at ambient temperature. After stirring overnight, methanol (5 mL) was added and the reaction was concentrated. Chromatography on SiO2 (7.2 g) using 1:2 hexane/ethyl acetate afforded 5-(N′-(ethoxycarbonylmethyl)ureido)-3-[1-(pyrrol-2-yl)ethylidene]indolin-2-one; 1H NMR (400 MHz, DMSO-d6) δ 1.32 (t, 3H), 2.82 (s, 3H), 3.96 (d, 2H), 4.22 (q, 2H), 6.44 (m, 2H), 6.88 (d, 1H), 7.16 (m, 1H), 7.28 (d, 1H), 7.40 (m, 1H), 7.96 (m, 1H), 8.76 (s, 1H), 11.02 (s, 1H) ppm; (200 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07105563B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-0314a4b9f2a34d77b81c20f8411fba5b |
| Source note | uspto-grants-2006_09 |