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Triethylamine → Pyrimidine-5-carboxylic acid{1-[2-chloro-4-(2-chloro-phenoxy)-benzyl-carbamoyl]-cyclopropyl}-amide

HRID 1406351
ノート
印刷プレビュー

反応式

HRID 1406351 の反応式
C(N(CC)CC)C.CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.[Cl:30][C:31]1[CH:38]=[C:37]([O:39][C:40]2[CH:45]=[CH:44][CH:43]=[CH:42][C:41]=2[Cl:46])[CH:36]=[CH:35][C:32]=1[CH2:33][NH2:34].[N:47]1[CH:52]=[C:51]([C:53]([NH:55][C:56]2([C:59](O)=[O:60])[CH2:58][CH2:57]2)=[O:54])[CH:50]=[N:49][CH:48]=1>O1CCCC1.CN(C=O)C>[Cl:30][C:31]1[CH:38]=[C:37]([O:39][C:40]2[CH:45]=[CH:44][CH:43]=[CH:42][C:41]=2[Cl:46])[CH:36]=[CH:35][C:32]=1[CH2:33][NH:34][C:59]([C:56]1([NH:55][C:53]([C:51]2[CH:50]=[N:49][CH:48]=[N:47][CH:52]=2)=[O:54])[CH2:58][CH2:57]1)=[O:60]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 8471TriethylamineHCID 2733207O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 584879012-Chloro-4-(2-chloro-phenoxy)-benzylamineHCID 594962911-[(Pyrimidine-5-carbonyl)-amino]cyclopropanecarboxylic acid

生成物 1

HCID 58487801Pyrimidine-5-carboxylic acid{1-[2-chloro-4-(2-chloro-phenoxy)-benzyl-carbamoyl]-cyclopropyl}-amide収率 29%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

85 mg (0.84 mmol) of triethylamine, 130 mg (0.40 mmol) of TBTU and 100 mg (0.37 mmol) of 2-chloro-4-(2-chloro-phenoxy)-benzylamine were added to a solution of 80 mg (0.38 mmol) of 1-[(pyrimidin-5-carbonyl)-amino]-cyclopropanecarboxylic acid (from 1 b) in 30 mL tetrahydrofuran and 5 mL DMF and the mixture was stirred overnight at ambient temperature. Then the mixture was evaporated to dryness and the residue was combined with 2 M potassium carbonate solution. It was extracted with ethyl acetate and the organic phase was washed with water and saturated sodium chloride solution, dried and evaporated down. The crude product thus obtained was purified by reversed-phase chromatography. The fractions were evaporated down to the aqueous phase, made basic with ammonia and extracted with ethyl acetate. The organic phase was washed with saturated sodium chloride solution, dried and evaporated down. The residue was evaporated out with ether and dried.

後処理

  1. customThen the mixture was evaporated to dryness
  2. extractionIt was extracted with ethyl acetate
  3. washthe organic phase was washed with water and saturated sodium chloride solution
  4. customdried
  5. customevaporated down

出典と根拠

ORDレコード
ord-68fbdd75702b48309474722479d9365a
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08916589B2

反応ノート

読み込み中…

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