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HRID 9123作成日:2026年10月26日

Triphenylphosphine → 1-(7-Vinyl-2-benzothiazolyl)-3-ethylurea

https://huagongshe.com/reaction/9123

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物TetravinylstannaneHCID 66189—
反応物Lithium ChlorideHCID 433294—
反応物1-(7-Trifluoromethylsulfonyl-2-benzothiazolyl)-3-ethylureaHCID 21985552—
触媒HCID 178418476HCID 178418476—
生成物1-(7-Vinyl-2-benzothiazolyl)-3-ethylureaHCID 2198560224.5%

反応条件

温度100 °C

反応手順

Similar to the synthesis of Example 203, a mixture of 1-(7-trifluoromethylsulfonyl-2-benzothiazolyl)-3-ethylurea (0.050 g, 80% pure, 0.11 mmol), lithium chloride (0.039 g, 0.92 mmol, 8.4 eq), triphenylphosphine (0.017 g, 0.066 mmol, 0.6 eq), Pd(PPh3)2Cl2 (0.009 g, 0.013 mmol, 0.12 eq), tetravinyltin (0.040 mL, 0.22 mmol, 2.0 eq), and a crystal of 2,6-di-tert-butyl-4-methylphenol was purged with nitrogen gas, and was heated at about 100° C. for about 1.5 hours. The mixture was taken up in MeOH, filtered, concentrated, and purified by HPLC and preparative TLC in ethyl acetate/heptane mixture to obtain 0.004 g (14%) of the desired compound. LC/MS 248 (M+1); LC retention time 2.96 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091227B2
出典データセットuspto-grants-2006_08
ORD IDord-1b2a9a1d73d34afbbad146c0399680cb
出典メモuspto-grants-2006_08