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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 722714생성일: 2026년 10월 26일

2-amino-4H,5H,6H-cyclopenta(b)thiophene-3-carbonitrile → 3-Methyl-2-phenyl-pentanoic acid (3-cyano-5,6-dihydro-4H-cyclopenta[b]thiophen-2-yl)-amide

https://huagongshe.com/reaction/722714

반응식

참여 물질

역할이름HCID투입량
반응물2-amino-4H,5H,6H-cyclopenta(b)thiophene-3-carbonitrileHCID 258182—
반응물3-Methyl-2-phenylvaleryl chlorideHCID 21886026—
생성물3-Methyl-2-phenyl-pentanoic acid (3-cyano-5,6-dihydro-4H-cyclopenta[b]thiophen-2-yl)-amideHCID 11393603—

반응 단계

Reaction of 3-methyl-2-phenylvaleryl chloride (Prepared in Example 7, Step1) and 2-Amino-3-cyano-5,6-dihydro-4H-cyclopenta[b]thiophene (164 mg; 1.0 mmol) according to the procedure outlined in Example 5 for 20 h at room temperature provided after workup, crude which triturated with diethylether to give 94 mg of crude 3-Methyl-2-phenyl-pentanoic acid (3-cyano-5,6-dihydro-4H-cyclopenta[b]thiophen-2-yl)-amide which was further purified by dissolving in methylene chloride and passing through a short plug of Merck Silica gel 60 to provide 82 mg (24%) of 3-Methyl-2-phenyl-pentanoic acid (3-cyano-5,6-dihydro-4H-cyclopenta[b]thiophen-2-yl)-amide as a mixture of diastereomers. ES-HRMS m/e calcd for C26H38N2O2 (M+Ht) 411.3006, found 411.3011.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07138529B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-0b9368bdcff74ac98b7c4f8a337b30ef
출처 메모uspto-grants-2006_11