HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Azetidinyl(4-bromo-2-fluorophenyl)methanone → HCID 59560327, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Azetidinyl(4-bromo-2-fluorophenyl)methanone | HCID 59351120 | — |
| Reactant | Methyl 6-hydroxy-2,2-dimethyl-2,3-dihydro-1-benzofuran-4-carboxylate | HCID 59560026 | — |
| Reactant | 4-[4-(Azetidine-1-carbonyl)-phenoxy]-2,2-dimethyl-2,3-dihydro-benzofuran-6-carboxylic acid methyl ester | HCID 59560251 | — |
| Product | HCID 59560327 | HCID 59560327 | — |
Reaction Steps
The title compound was prepared in a similar manner as described for Intermediate 35b, from azetidin-1-yl-(4-bromo-2-fluoro-phenyl)-methanone and 6-hydroxy-2,2-dimethyl-2,3-dihydro-benzofuran-4-carboxylic acid methyl ester (197e). 1H NMR (400 MHz, CDCl3) δ 7.42 (d, J=7.07 Hz, 1 H) 7.37 (d, J=1.77 Hz, 1 H) 7.29 (dd, J=9.35, 1.52 Hz, 1 H) 7.15 (d, J=2.27 Hz, 1 H) 6.62 (d, J=2.27 Hz, 1 H) 4.16-4.25 (m, 2 H) 4.07-4.16 (m, 2 H) 3.87-3.88 (m, 3 H) 3.33 (s, 2 H) 2.29-2.39 (m, 2 H) 1.51 (s, 6 H); LCMS for C22H22FNO5 m/z 441.30 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119624B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-21cec7b353074fbc98bf99778a2c6fbc |
| Source note | uspto-grants-2012_02 |