HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102553Generated: October 31, 2026
4-Propoxypiperidine → (R)-4-[2-Methyl-3-(4-propoxypiperidin-1-yl)propyl]-4H-benzo[1,4]thiazin-3-one
https://huagongshe.com/reaction/2102553
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Propoxypiperidine | HCID 11492037 | — |
| Reactant | (S)-4-(3-Iodo-2-methylpropyl]-4H-benzo[1,4]thiazin-3-one | HCID 68910017 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (R)-4-[2-Methyl-3-(4-propoxypiperidin-1-yl)propyl]-4H-benzo[1,4]thiazin-3-one | HCID 10286975 | 49% |
Reaction Steps
The compound (S)-4-(3-Iodo-2-methyl-propyl]-4H-benzo[1,4]thiazin-3-one (108LM37-34) (0.433 g, 1.25 mmol) and 4-propoxypiperidine (79KS66) (0.225 g, 1.55 mmol) in MeCN (½ mL) were reacted according to GP10 shaking at 60° C. for 4 days. Purified by cation exchange CC and flash CC (SiO2; MeOH/DCM 1:20) to give the title compound (108LM49-46) (0.220 g, 49%). 1H NMR (CDCl3) δ 7.37 (d, J=8.1 Hz, 1H), 7.25-7.20 (m, 2H), 7.05-6.97 (m, 1H), 4.18-4.00 (m, 2H), 3.42-3.35 (m, 4H), 3.30-3.20 (m, 1H), 2.80-2.70 (m, 1H), 2.65-2.55 (m, 1H), 2.20-2.05 (m, 3H), 2.00-1.82 (m, 4H), 1.62-1.50 (m, 4H), 0.92 (t, J=7.4, CH3), 0.82 (d, J=6.8 Hz, CH3), 13C NMR (CDCl3) δ 166.1, 139.2, 128.8, 127.1, 124.9, 123.5, 118.8, 75.5, 69.8, 63.3, 52.7, 51.9, 47.6, 32.1, 32.0, 29.6, 23.5, 16.6, 10.9; HPLC-MS (ammonium acetate) [M+H]+=363.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576078B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-d4f5eef3e726453ba82ab4b05a215169 |
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| Source note | uspto-grants-2009_08 |
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