4-(benzyloxy)-7-bromo-5-fluoro-1-methyl-1H-indole → 6-bromo-7-propyl-3,7-dihydro-2H-[1,4]dioxino[2,3-e]indole

反応式

[CH2:1](OC1C(F)=CC(Br)=C2C=1C=CN2C)[C:2]1C=CC=C[CH:3]=1.[Br:21][C:22]1[CH:23]=[C:24]2[O:34][CH2:33][CH2:32][O:31][C:25]2=[C:26]2[C:30]=1[NH:29][CH:28]=[CH:27]2>>[Br:21][C:22]1[CH:23]=[C:24]2[O:34][CH2:33][CH2:32][O:31][C:25]2=[C:26]2[C:30]=1[N:29]([CH2:1][CH2:2][CH3:3])[CH:28]=[CH:27]2

参加物

反応物 2

HCID 583039584-(benzyloxy)-7-bromo-5-fluoro-1-methyl-1H-indole

HCID 669271316-bromo-3,7-dihydro-2H-[1,4]dioxino[2,3-e]indole

生成物 1

HCID 669272196-bromo-7-propyl-3,7-dihydro-2H-[1,4]dioxino[2,3-e]indole収率 90%

実験手順

Following the procedure (step 2, scheme 33) used to prepare compound 33-3, compound 40-2 gave compound 40-3 in 90% yield as a yellow solid. LCMS: calc 295.0 found 296.0 [MH]+.

出典と根拠

ORDレコード: ord-2768aac443b44f7bbf9278d51641dd9e
出典データセット: uspto-grants-2014_12
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US08912220B2

反応ノート

読み込み中…