HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Bromopyridine-2-carbaldehyde → 4-[(6-Bromopyridin-2-yl)methyl]thiomorpholine 1,1-dioxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Bromopyridine-2-carbaldehyde | HCID 2757009 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Thiomorpholine 1,1-dioxide | HCID 6484228 | — |
| Product | 4-[(6-Bromopyridin-2-yl)methyl]thiomorpholine 1,1-dioxide | HCID 58335258 | — |
Reaction Steps
The title compound was prepared as described in Example 2, Step 1 using 6-bromopyridine-2-carbaldehyde (3.0 g, 16.13 mmol), thiomorpholine 1,1-dioxide (2.18 g, 16.13 mmol), and sodium triacetoxyborohydride (4.79 g, 22.58 mmol) as starting materials. 1H NMR (600 MHz, d6-DMSO) δ 7.72 (t, 1H), 7.51 (d, 1H), 7.50 (d, 1H), 3.74 (s, 2H), 3.10 (m, 4H), 2.90 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08278335B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-e6ac2623d6a4454f8c8742cd484d2790 |
| Source note | uspto-grants-2012_10 |