HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Ethynylbenzo-1,3-dioxole → Ethyl 3-(2H-1,3-benzodioxol-5-yl)prop-2-ynoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Ethynylbenzo-1,3-dioxole | HCID 92680 | — |
| Reactant | 7-[2-(1H-indol-5-yloxy)-ethyl]-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl ester | HCID 66821083 | — |
| Product | Ethyl 3-(2H-1,3-benzodioxol-5-yl)prop-2-ynoate | HCID 11275992 | 54% |
Reaction Steps
The title compound was synthesized from 5-ethynyl-benzo[1,3]dioxole and 7-[2-(1H-indol-5-yloxy)-ethyl]-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl ester using the procedure described in Example 23, step (c), in 54% yield. 1H NMR (CDCl3) δ 7.16 (dd, 1H, J=1.6, 8.1 Hz), 7.00 (d, 1H, J=1.6 Hz,), 6.80 (d, 1H, J=8.1 Hz,), 6.02 (s, 2H), 4.29 (q, 2H, J=7.2 Hz,), 1.35 (t, 3H, J=7.2 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06855722B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-a9e91db964a846f08d7ccdceb8e8220e |
| Source note | uspto-grants-2005_02 |