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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 345165생성일: 2026년 10월 25일

Indoline → 1,2,3,4-Tetrahydroisoquinoline

https://huagongshe.com/reaction/345165

반응식

참여 물질

역할이름HCID투입량
반응물IndolineHCID 10328—
반응물ThiazolidineHCID 10444—
반응물PyrrolidineHCID 31268—
반응물DecahydroisoquinolineHCID 97812—
반응물Octahydro-1H-indoleHCID 107275—
반응물Octahydrocyclopenta(c)pyrroleHCID 110688—
반응물OctahydroisoindoleHCID 409979—
반응물2-Azaspiro(4.5)decaneHCID 418822—
반응물2-Azaspiro(4.4)nonaneHCID 418904—
반응물Octahydrocyclopenta[B]pyrroleHCID 12400272—
반응물2-Azabicyclo[3.1.0]hexaneHCID 17783223—
반응물2,3,3a,4,5,7a-HexahydroindoleHCID 18426479—
반응물Decahydrocyclohepta[b]pyrroleHCID 18925332—
반응물2-Azatricyclo[4.3.0.16,9]decaneHCID 55298740—
생성물1,2,3,4-TetrahydroisoquinolineHCID 7046—

반응 단계

decahydroisoquinoline (B); octahydroindole (C); octahydrocyclopenta[b]pyrrole (D); 2-azaspiro[4.5]decane (E); 2-azaspiro[4.4]-nonane (F); spiro[(bicyclo[2.2.1]heptane)-2,3'-pyrrolidine] (G); spiro[(bicyclo[2.2.2]octane)-2,3'-pyrrolidine] (H); 2-azatricyclo[4.3.0.16,9 ]decane (I); decahydrocyclohepta[b]pyrrole (J); hexahydrocyclopropa[b]pyrrole (K); octahydroisoindole (L); octahydrocyclopenta[c]pyrrole (M); 2,3,3a,4,5,7a-hexahydroindole (N); 1,2,3,3a,4,6ahexahydrocyclopenta[b]pyrrole (O); pyrrolidine (P); indoline (Q) and thiazolidine (R), all of which can be optionally substituted.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05055483
출처 데이터셋uspto-grants-1991_10
ORD IDord-fa8a8018ccdb46f39356b6f9ebac9b1f
출처 메모uspto-grants-1991_10