Acetic Acid → (9-(2,3-Difluoro-5-(2-hydroxyethyl)benzyl)-1-oxa-4,9-diazaspiro[5.5]undecan-4-yl)(5-methylthiophen-2-yl)methanone

HRID 471035ノート

反応式

HRID 471035 の反応式
FC(F)(F)C(O)=O.[CH3:8][C:9]1[S:13][C:12]([C:14]([N:16]2[CH2:21][C:20]3([CH2:26][CH2:25][NH:24][CH2:23][CH2:22]3)[O:19][CH2:18][CH2:17]2)=[O:15])=[CH:11][CH:10]=1.[F:27][C:28]1[C:35]([F:36])=[CH:34][C:33]([CH2:37][CH2:38][OH:39])=[CH:32][C:29]=1[CH:30]=O.C(O)(=O)C.C([BH3-])#N.[Na+]>CO>[F:27][C:28]1[C:35]([F:36])=[CH:34][C:33]([CH2:37][CH2:38][OH:39])=[CH:32][C:29]=1[CH2:30][N:24]1[CH2:25][CH2:26][C:20]2([O:19][CH2:18][CH2:17][N:16]([C:14]([C:12]3[S:13][C:9]([CH3:8])=[CH:10][CH:11]=3)=[O:15])[CH2:21]2)[CH2:22][CH2:23]1

参加物

6

実験手順

(5-Methylthiophen-2-yl)(1-oxa-4,9-diazaspiro[5.5]undecan-4-yl)methanone trifluoroacetate (example 9, step b) (0.53 g) was added to a solution of 2,3-difluoro-5-(2-hydroxyethyl)benzaldehyde (example 32, step b) (0.25 g) and acetic acid (0.08 mL) in methanol (5 mL). The reaction was stirred for 30 min and cooled in an ice bath. Sodium cyanoborohydride (0.13 g) was then added, the mixture allowed to warm to RT and stirred for 18 h. The reaction was concentrated in vacuo. Purification was by silica gel chromatography eluting with 99:1:0.1 to 97:3:0.3 DCM:methanol:‘880’ aqueous ammonia gradient. The fractions containing product were combined and evaporated in vacuo to give the subtitled compound as a gum. Yield 0.08 g.

後処理

  1. temperaturecooled in an ice bath
  2. stirringstirred for 18 h
  3. concentrationThe reaction was concentrated in vacuo
  4. customPurification
  5. washeluting with 99:1:0.1 to 97:3:0.3 DCM
  6. additionThe fractions containing product
  7. customevaporated in vacuo

出典と根拠

ORDレコード
ord-769cbfe0950b44d19a184d94401d6f24
出典データセット
uspto-grants-2014_01
特許番号
US08629271B2

反応ノート

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