碘化油 → 3-(4,4-difluorocyclohexyl)-2-(5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-N-(5-methoxythiazolo[5,4-b]pyridin-2-yl)propionamide

HRID 14998

反应方程式

HRID 14998 反应方程式
C([O:3][C:4]([CH2:6][C:7]1[CH:20]=[CH:19][C:18]2[S:17](=[O:22])(=[O:21])[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[N:10](C(OC(C)(C)C)=O)[C:9]=2[CH:8]=1)=O)C.[F:30][C:31]1([F:39])[CH2:36][CH2:35][CH:34]([CH2:37]I)[CH2:33][CH2:32]1.FC1(F)CCC(C(OCC)=O)CC1.[I-].[CH3:54][O:55][C:56]1[N:61]=[C:60]2[S:62][C:63]([NH2:65])=[N:64][C:59]2=[CH:58][CH:57]=1>>[F:30][C:31]1([F:39])[CH2:36][CH2:35][CH:34]([CH2:37][CH:6]([C:7]2[CH:20]=[CH:19][C:18]3[S:17](=[O:22])(=[O:21])[C:16]4[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=4)[NH:10][C:9]=3[CH:8]=2)[C:4]([NH:65][C:63]2[S:62][C:60]3[C:59]([N:64]=2)=[CH:58][CH:57]=[C:56]([O:55][CH3:54])[N:61]=3)=[O:3])[CH2:33][CH2:32]1

参与物

6

反应物 5

HCID 30165碘化油HCID 2779138乙基-4,4-二氟环己烷羧酸盐HCID 28015575-甲氧基三阿咪唑HCID 59340981tert-butyl 2-ethoxycarbonylmethyl-5,5-dioxo-5H-phenothiazine-10-carboxylateHCID 672369851,1-Difluoro-4-(iodomethyl)cyclohexane

产物 1

HCID 580242543-(4,4-difluorocyclohexyl)-2-(5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-N-(5-methoxythiazolo[5,4-b]pyridin-2-yl)propionamide

实验过程

Analogously to Example 36 and Example 44, tert-butyl 2-ethoxycarbonylmethyl-5,5-dioxo-5H-phenothiazine-10-carboxylate, 1,1-difluoro-4-iodomethylcyclohexane (prepared from commercially available ethyl 4,4-difluorocyclohexanecarboxylate analogously to the synthesis of the iodide described in Example 40) and 5-methoxy-thiazolo[5,4-b]pyridin-2-ylamine give 3-(4,4-difluorocyclohexyl)-2-(5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-N-(5-methoxythiazolo[5,4-b]pyridin-2-yl)propionamide.

来源与证据

ORD记录
ord-3958a078b667471db485796a4948a9a2
来源数据集
uspto-grants-2010_06
专利号
US07732440B2

关联笔记

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