HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585598Generated: October 26, 2026
Sodium hydride → 2-amino-5-(Benzothiazol-2-ylmethoxy)-naphthalene
https://huagongshe.com/reaction/585598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Aminonaphthol | HCID 90295 | — |
| Reactant | 2-(Bromomethyl)-1,3-benzothiazole | HCID 2776258 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-amino-5-(Benzothiazol-2-ylmethoxy)-naphthalene | HCID 22337844 | 15% |
Reaction Steps
Sodium hydride (1.05 g) is added to a cooled solution of 2-Amino-5-naphthol (4.18 g) in dimethylformamide (100 mL). Stir at room temperature 15 minutes and cool mixture. 2-Bromomethylbenzothiazole (6.00 g) is added and mixture to allowed to warm slowly and stir for 24 hours. Remove dimethylformamide in vacuo. Redilute with ethylacetate and absorb onto silica gel. Chromatograph (ethyl acetate/hexane) to give a brown solid (1.20 g, 15%) which was used directly in the next step., m.p. 141-143° C. 1H NMR (DMSO-d6, 400 MHz): d 5.43 (br s, 2H), 5.69 (s, 2H), 6.72 (d, 1H), 6.80 (s, 1H), 6.95 (d, 1H), 7.12-7.20 (m, 2H), 7.45 (t, 1H), 7.54 (t, 1H), 7.97 (d, 1H), 8.02 (d, 1H), 8.14 (d, 1H). MS [EI, m/z]: 306 [M]+. Anal. Calcd. for C18H14N2OS: C, 70.56; H, 4.61; N, 9.14. Found: C, 70.38; H, 4.42; N, 9.25.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06933322B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-c1f8f064938c45a98ca03e770979bd78 |
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| Source note | uspto-grants-2005_08 |
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