HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nicotinamide → HCID 14986521, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nicotinamide | HCID 936 | — |
| Reactant | 3-Methoxythiophene | HCID 140249 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | 6-bromo-5,6-dihydro-7-hydroxy-5,5-dimethyl-7H-thieno[3,2-b]pyran | HCID 14986486 | — |
| Product | HCID 14986521 | HCID 14986521 | — |
Reaction Steps
The title compound was prepared as described for Example 3 starting with 6-bromo-5,6-dihydro-7-hydroxy-5,5-dimethyl-7H -thieno[3,2-b]pyran (4.0 g, 15.2 mmol) and nicotinamide (3.7 g, 30.4 mmol) to give 1.1 g (24%): m.p. 248°-49° C.; IR (KBr): 3329, 3312,1648, 1594, 1569 cm-1 ; MS: m/z 305 (MH+); 1 1H NMR (CDCl3) 6 9.02 (s, 1H), 8.79 (d, J=5,6 Hz, 1H), 8.14 (d, J=5,6 Hz, 1H), 7.44 (m, 1H), 7.18 (d, J=5.4 Hz, 1H), 6.64 (d, J=5.4 Hz, 1H), 6.55 (d, J=5,6, 1H), 5.20 (m, 1H), 4.46 (brs, 1H), 3.81 (d, J=9.4 Hz, 1H), 1.50 (s, 3H), 1.36 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05284857 |
| Source dataset | uspto-grants-1994_02 |
| ORD ID | ord-17a2d55af877497ca73fbc80498cd11c |
| Source note | uspto-grants-1994_02 |