HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → HCID 20767893, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 22143552 | HCID 22143552 | — |
| Product | HCID 20767893 | HCID 20767893 | — |
Reaction Steps
This material was prepared from 6-[2-(3-methoxypyrrolidine-1-carbonyl)-thieno[3,2-b]pyridin-7-yloxy]-2-methyl-benzofuran-3-carboxylic acid 89e by treatment with oxalyl chloride and 2-aminoethanol in a manner as previously described for example 16d. 1H NMR (DMSO-d6) δ8.57 (1H, d, J=5.6 Hz), 8.06 (1H, s), 8.00 (1H, t, J=5.3 Hz), 7.82 (1H, d, J=8.6 Hz), 7.66 (1H, d, J=2.3 Hz), 7.26 (1H, dd, J=8.3, 2.3 Hz), 6.72 (1H, d, J=5.3 Hz), 4.76(1H, m), 4.10-3.82 (3H, m), 3.67-3.59 (2H, m), 3.55 (2H, t, J=6.1 Hz), 3.37 (2H, t, J=6.1 Hz), 3.27, 3.24 (3H, 2s), 2.63 (3H, s), 2.06 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06869962B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-feb3d60cacd947a38caea82b370c1e9f |
| Source note | uspto-grants-2005_03 |