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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1806449생성일: 2026년 10월 25일

(S)-(+)-Tetrahydrofurfurylamine → 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-[3-fluoro-5-({[(2S)-2-methylbutyl]amino}methyl)phenyl]-1H-indole-7-carboxamide trifluoroacetate

https://huagongshe.com/reaction/1806449

반응식

참여 물질

역할이름HCID투입량
반응물(S)-(+)-TetrahydrofurfurylamineHCID 641530—
반응물3-[1-(ethylsulfonyl)-4-piperidinyl]-5-[3-fluoro-5-({[(2S)-tetrahydro-2-furanylmethyl]amino}methyl)phenyl]-1H-indole-7-carboxamide trifluoroacetateHCID 66723136—
생성물3-[1-(ethylsulfonyl)-4-piperidinyl]-5-[3-fluoro-5-({[(2S)-2-methylbutyl]amino}methyl)phenyl]-1H-indole-7-carboxamide trifluoroacetateHCID 6672336641.7%

반응 단계

The title compound was prepared according to the general procedure of 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-[3-fluoro-5-({[(2S)-tetrahydro-2-furanylmethyl]amino}methyl)phenyl]-1H-indole-7-carboxamide trifluoroacetate, substituting (2S)-2-methyl-1-butanamine (45 mg, 0.525 mmol) for 1-[(2S)-tetrahydro-2-furanyl]methanamine to afford 23.3 mg of the title compound (41.7%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08354406B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-20d6770158a24d31a2676db40e9b1635
출처 메모uspto-grants-2013_01