HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330801Generated: October 29, 2026
Triphenylphosphine → 3-{3-[5-(3-dimethylaminopropoxy)pyrimidin-2-yl]benzyl}-5-trifluoromethyl-3H-benzothiazol-2-one
https://huagongshe.com/reaction/330801
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| Reactant | 5-(Trifluoromethyl)benzo[d]thiazol-2(3H)-one | HCID 13227340 | — |
| Reactant | {3-[5-(3-Dimethylaminopropoxy)pyrimidin-2-yl]phenyl}methanol | HCID 59484942 | — |
| Product | 3-{3-[5-(3-dimethylaminopropoxy)pyrimidin-2-yl]benzyl}-5-trifluoromethyl-3H-benzothiazol-2-one | HCID 46846628 | — |
Reaction Steps
A suspension of 114 mg (0.52 mmol) of 5-trifluoromethyl-3H-benzothiazol-2-one, 150 mg (0.52 mmol) of {3-[5-(3-dimethylaminopropoxy)pyrimidin-2-yl]phenyl}methanol and 261 mg (0.78 mmol) of polymer-bound triphenylphosphine (3mmol/g) is shaken at room temperature for 30 min. 178 mg (0.78 mmol) of di-tert-butyl azodicarboxylate are added to the suspension, and, after the mixture has been stirred at room temperature for 24 h, 50 mg (0.15 mmol) of polymer-bound triphenylphosphine (3 mmol/g) and 35 mg (0.15 mmol) of di-tert-butyl azodicarboxylate are again present and shaken at room temperature for 2 h. The reaction mixture is filtered, the filtrate is evaporated to dryness, and the residue is purified by means of preparative HPLC. The product is in the form of the trifluoroacetate; ESI: 489 (M+H); Rt.=2.81 min (method A);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877751B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-f937e100eef7407481c2c51dceb0527a |
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| Source note | uspto-grants-2014_11 |
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