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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 218802생성일: 2026년 10월 24일

2-Chloro-5-(chloromethyl)thiophene → 5-benzyloxy-N-({1-[(5-chlorothiophen-2-yl)methyl]pyrazol-4-yl}methyl)-N-(6-isopropylpyridin-3-yl)-1,2,3,4-tetrahydronaphthalene-1-carboxamide

https://huagongshe.com/ko/reaction/218802

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloro-5-(chloromethyl)thiopheneHCID 583079—
반응물5-benzyloxy-N-(6-isopropylpyridin-3-yl)-N-[(pyrazol-4-yl)methyl]-1,2,3,4-tetrahydronaphthalene-1-carboxamideHCID 59597432—
생성물5-benzyloxy-N-({1-[(5-chlorothiophen-2-yl)methyl]pyrazol-4-yl}methyl)-N-(6-isopropylpyridin-3-yl)-1,2,3,4-tetrahydronaphthalene-1-carboxamideHCID 6718479474.8%

반응 단계

By the reaction and treatment in the same manner as in Example 83 using 5-benzyloxy-N-(6-isopropylpyridin-3-yl)-N-[(pyrazol-4-yl)methyl]-1,2,3,4-tetrahydronaphthalene-1-carboxamide (1.44 g) and 2-chloro-5-(chloromethyl)thiophene (0.79 g) as starting materials, 5-benzyloxy-N-({1-[(5-chlorothiophen-2-yl)methyl]pyrazol-4-yl}methyl)-N-(6-isopropylpyridin-3-yl)-1,2,3,4-tetrahydronaphthalene-1-carboxamide (1.37 g) was obtained. By the reaction and treatment of this compound in the same manner as in Example 133, N-({1-[(5-chlorothiophen-2-yl)methyl]pyrazol-4-yl}methyl)-5-hydroxy-N-(6-isopropylpyridin-3-yl)-1,2,3,4-tetrahydronaphthalene-1-carboxamide (0.37 g) was obtained. melting point: 98-101° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198454B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-b3db4f1e6e304c7bbec42e49faaf18eb
출처 메모uspto-grants-2012_06