HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9122Generated: October 25, 2026
Chlorosuccinimide → 1-(7-Isopropoxy-2-benzothiazolyl)-3-ethylurea
https://huagongshe.com/reaction/9122
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 1-(6-Bromo-7-isopropoxy-2-benzothiazolyl)-3-ethylurea | HCID 21985546 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 1-(7-Isopropoxy-2-benzothiazolyl)-3-ethylurea | HCID 21985653 | 25.1% |
Reaction Steps
A solution of 1-(6-bromo-7-isopropoxy-2-benzothiazolyl)-3-ethylurea (0.036 g, 0.10 mmol) in 0.5 mL DME was cooled down to about −78° C., and was treated with a solution of 1.6 M n-BuLi in hexanes (0.16 mL, 0.26 mmol, 2.6 eq). It was stirred at the temperature for about 20 min, then a solution of N-chlorosuccinimide (NCS) (0.015 g, 0.11 mmol, 1.1 eq) in 0.5 mL DME was added. It was warmed up to about 0° C. for about 0.5 hour. It was taken up in MeOH and purified by HPLC to give 0.007 g (25%) of the title compound. LC/MS 279.9 (M+1); LC retention time 3.10 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07091227B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-9a4c0e1c1fc94c6586402782e0c32725 |
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| Source note | uspto-grants-2006_08 |
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