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HRID 23985作成日:2026年10月24日

Tributylphosphine → Methyl 3-{5-[3-(benzyloxycarbonylamino)propoxy]-indolyl}propanoate

https://huagongshe.com/ja/reaction/23985

反応式

関与物質

役割名称HCID仕込み量
反応物TributylphosphineHCID 13831—
反応物1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
反応物Benzyl N-(3-hydroxypropyl)carbamateHCID 562256—
反応物methyl 3-(5-hydroxy-1H-indol-2-yl)propanoateHCID 22570384—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 3-{5-[3-(benzyloxycarbonylamino)propoxy]-indolyl}propanoateHCID 22570338—

反応手順

1,1′-(Azodicarbonyl)dipiperidine (370 mg, 1.5 mmol) was added to the solution of methyl 3-(5-hydroxyindolyl)propanoate (220 mg, 1.0 mmol), as prepared in step g of Example 5, 3-(benzyloxycarbonylamino)propanol (230 mg, 1.1 mmol) and tri-n-butylphosphine (305 mg, 1.5 mmol) in tetrahydrofuran (20 mL). After stirring at ambient temperature overnight, the reaction mixture was concentrated and the residue was purified by flash column chromatography on silica gel (0-2% ethyl acetate in methylene chloride) to give the title compound as an off white solid (310 mg, 76%). 1H-NMR (400 MHz, CDCl3) δ 7.35 (m, 5H), 7.22 (d, J=8.9 Hz, 1H), 7.09 (d, J=3.1 Hz, 1H), 7.07 (d, J=2.1 Hz, 1H), 6.86 (dd, J=8.8, 2.4 Hz, 1H), 6.38 (d, J=2.9 Hz, 1H), 5.11 (br s, 3H), 4.41 (t, J=6.8 Hz, 2H), 4.07 (t, J=5.9 Hz, 2H), 3.66 (s, 3H), 3.44 (q, J=6.3 Hz, 2H), 2.81 (t, J=6.8 Hz, 2H), 2.02 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855722B2
出典データセットuspto-grants-2005_02
ORD IDord-b7e30da35c9f479082ec3a09dcec3b98
出典メモuspto-grants-2005_02