HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Ethynylcyclopentanol → HCID 71714693, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Ethynylcyclopentanol | HCID 87074 | — |
| Reactant | 10-Bromo-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamide | HCID 68312883 | — |
| Product | HCID 71714693 | HCID 71714693 | — |
Reaction Steps
10-Bromo-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamide (0.1 g) was reacted with 1-ethynylcyclopentanol similar to as described in Procedure E to afford 22.4 mg of 10-[2-(1-hydroxycyclopentyl)ethynyl]-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamide following reverse phase hplc purification. MS (Q1) 338 (M)+. 1H NMR (400 MHz, DMSO) δ 8.50 (d, J=2.1 Hz, 1H), 7.84-7.71 (m, 1H), 7.54 (d, J=23.6 Hz, 1H), 7.29 (dd, J=8.5, 2.1 Hz, 1H), 7.10 (s, 1H), 7.01 (d, J=8.5 Hz, 1H), 5.28 (s, 1H), 4.49 (d, J=12.6 Hz, 4H), 1.94-1.84 (m, 4H), 1.82-1.62 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09034866B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-b53f5e26d73d48e2a2ad8c754f93f0cc |
| Source note | uspto-grants-2015_05 |