Dibah → 2-chloro-5-fluoro-N4-(1,2,3,4-tetrahydro-1-hydroxynaphthalen-7-yl)-4-pyrimidineamine

HRID 226592

反応式

HRID 226592 の反応式
C1COC2(N)N(C(NC3C=CC4OC(CO)=CC=4C=3)=NC=C2F)O1.[Cl:25][C:26]1[N:31]=[C:30]([NH:32][C:33]2[CH:42]=[C:41]3[C:36]([CH2:37][CH2:38][CH2:39][C:40]3=[O:43])=[CH:35][CH:34]=2)[C:29]([F:44])=[CH:28][N:27]=1.CC(C[Al]CC(C)C)C>>[Cl:25][C:26]1[N:31]=[C:30]([NH:32][C:33]2[CH:42]=[C:41]3[C:36]([CH2:37][CH2:38][CH2:39][CH:40]3[OH:43])=[CH:35][CH:34]=2)[C:29]([F:44])=[CH:28][N:27]=1

参加物

4

反応物 3

HCID 16682954DibahHCID 220607872-chloro-5-fluoro-N4-(1,2,3,4-tetrahydro-1-oxonaphthalen-7-yl)-4-pyrimidineamineHCID 66759177N4-(3,4-ethylenedioxy)-5-fluoro-N2-[2-(hydroxymethyl)benzofuran-5-yl]-2,4-pyrimidinediamine

生成物 1

HCID 220608542-chloro-5-fluoro-N4-(1,2,3,4-tetrahydro-1-hydroxynaphthalen-7-yl)-4-pyrimidineamine

実験手順

In a manner similar to the preparation of N4-(3,4-ethylenedioxy)-5-fluoro-N2-[2-(hydroxymethyl)benzofuran-5-yl]-2,4-pyrimidinediamine, 2-chloro-5-fluoro-N4-(1,2,3,4-tetrahydro-1-oxonaphthalen-7-yl)-4-pyrimidineamine was reduced with Dibal-H to yield 2-chloro-5-fluoro-N4-(1,2,3,4-tetrahydro-1-hydroxynaphthalen-7-yl)-4-pyrimidineamine.

出典と根拠

ORDレコード
ord-80c65d180bcf49589d54026f79d408cb
出典データセット
uspto-grants-2009_07
特許番号
US07557210B2

関連ノート

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