One-Pot Synthesis of 2′-Aminobenzothiazolo-Arylmethyl-2-Naphthols Catalyzed by NBS under Solvent-Free Conditions
To develop a new facile protocol for the synthesis of 2′-aminobenzothiazolo-arylmethyl-2-naphthol derivatives, N-bromosuccinimide (NBS) was used as an efficient catalyst for the one-pot synthesis of 2′-aminobenzothiazolo-arylmethyl-2-naphthols in excellent yields from β-naphthol (1 mmol), aromatic a...
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| Format: | Article |
| Language: | English |
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Wiley
2013-01-01
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| Series: | The Scientific World Journal |
| Online Access: | http://dx.doi.org/10.1155/2013/702929 |
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| _version_ | 1832567544791171072 |
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| author | Wei Lin Li Li Li Wang Qiu Yan Luo |
| author_facet | Wei Lin Li Li Li Wang Qiu Yan Luo |
| author_sort | Wei Lin Li |
| collection | DOAJ |
| description | To develop a new facile protocol for the synthesis of 2′-aminobenzothiazolo-arylmethyl-2-naphthol derivatives, N-bromosuccinimide (NBS) was used as an efficient catalyst for the one-pot synthesis of 2′-aminobenzothiazolo-arylmethyl-2-naphthols in excellent yields from β-naphthol (1 mmol), aromatic aldehydes (1 mmol), and 2-aminobenzothiazole (1 mmol) at 60°C under solvent-free conditions. |
| format | Article |
| id | doaj-art-c1aa896756974186a11336190305cd80 |
| institution | Kabale University |
| issn | 1537-744X |
| language | English |
| publishDate | 2013-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | The Scientific World Journal |
| spelling | doaj-art-c1aa896756974186a11336190305cd802025-02-03T01:01:15ZengWileyThe Scientific World Journal1537-744X2013-01-01201310.1155/2013/702929702929One-Pot Synthesis of 2′-Aminobenzothiazolo-Arylmethyl-2-Naphthols Catalyzed by NBS under Solvent-Free ConditionsWei Lin Li0Li Li Wang1Qiu Yan Luo2Department of Medicinal Chemistry, Pharmacy College of Xinxiang Medical University, Xinxiang 453003, ChinaDepartment of Gynecological and Obstetric, The Third Affiliated Hospital of Xinxiang Medical College, Xinxiang 453003, ChinaDepartment of Gynecological and Obstetric, The Third Affiliated Hospital of Xinxiang Medical College, Xinxiang 453003, ChinaTo develop a new facile protocol for the synthesis of 2′-aminobenzothiazolo-arylmethyl-2-naphthol derivatives, N-bromosuccinimide (NBS) was used as an efficient catalyst for the one-pot synthesis of 2′-aminobenzothiazolo-arylmethyl-2-naphthols in excellent yields from β-naphthol (1 mmol), aromatic aldehydes (1 mmol), and 2-aminobenzothiazole (1 mmol) at 60°C under solvent-free conditions.http://dx.doi.org/10.1155/2013/702929 |
| spellingShingle | Wei Lin Li Li Li Wang Qiu Yan Luo One-Pot Synthesis of 2′-Aminobenzothiazolo-Arylmethyl-2-Naphthols Catalyzed by NBS under Solvent-Free Conditions The Scientific World Journal |
| title | One-Pot Synthesis of 2′-Aminobenzothiazolo-Arylmethyl-2-Naphthols Catalyzed by NBS under Solvent-Free Conditions |
| title_full | One-Pot Synthesis of 2′-Aminobenzothiazolo-Arylmethyl-2-Naphthols Catalyzed by NBS under Solvent-Free Conditions |
| title_fullStr | One-Pot Synthesis of 2′-Aminobenzothiazolo-Arylmethyl-2-Naphthols Catalyzed by NBS under Solvent-Free Conditions |
| title_full_unstemmed | One-Pot Synthesis of 2′-Aminobenzothiazolo-Arylmethyl-2-Naphthols Catalyzed by NBS under Solvent-Free Conditions |
| title_short | One-Pot Synthesis of 2′-Aminobenzothiazolo-Arylmethyl-2-Naphthols Catalyzed by NBS under Solvent-Free Conditions |
| title_sort | one pot synthesis of 2 aminobenzothiazolo arylmethyl 2 naphthols catalyzed by nbs under solvent free conditions |
| url | http://dx.doi.org/10.1155/2013/702929 |
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