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Hydrochloric Acid → HCID 10391157、化合物

HRID 736463
ノート
印刷プレビュー

反応式

HRID 736463 の反応式
C([Li])CCC.B(OC(C)C)(OC(C)C)OC(C)C.Br[C:20]1[CH:25]=[CH:24][C:23]([S:26]([N:29]2[CH2:33][CH2:32][CH2:31][CH2:30]2)(=[O:28])=[O:27])=[CH:22][CH:21]=1.[ClH:34].C(=O)([O-])[O-].[Na+].[Na+].[NH2:41][C:42]1[C:43]([C:49]([NH:51][CH2:52][CH2:53][N:54]2[CH2:59][CH2:58][O:57][CH2:56][CH2:55]2)=[O:50])=[N:44][C:45](Br)=[CH:46][N:47]=1>O1CCCC1.CO.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[ClH:34].[NH2:41][C:42]1[C:43]([C:49]([NH:51][CH2:52][CH2:53][N:54]2[CH2:59][CH2:58][O:57][CH2:56][CH2:55]2)=[O:50])=[N:44][C:45]([C:20]2[CH:25]=[CH:24][C:23]([S:26]([N:29]3[CH2:33][CH2:32][CH2:31][CH2:30]3)(=[O:28])=[O:27])=[CH:22][CH:21]=2)=[CH:46][N:47]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

10

反応物 6

HCID 313Hydrochloric Acid2 回HCID 10340Sodium CarbonateHCID 21531Triisopropyl borateHCID 7386181-(4-Bromobenzene-1-sulfonyl)pyrrolidineHCID 10426742HCID 10426742、化合物HCID 178418339Butyllithium

生成物 1

HCID 10391157
HCID 10391157、化合物
収率 26%

試薬・触媒・溶媒 3

HCID 44119782Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)触媒HCID 887Methanol溶媒HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-78 °C

実験手順

n-Butyllithium (1.6 mL, 2.6 mmol) was added dropwise over 10 min to a cooled solution (−78° C.) of triisopropyl borate (0.6 mL, 2.6 mmol), and 1-[(4-bromophenyl)sulfonyl]pyrrolidine (0.251 g, 0.86 mmol) in anhydrous tetrahydrofuran (10 mL) under an atmosphere of nitrogen. The resulting mixture was stirred at −78° C. for 1 h and the mixture was allowed to warm up to room temperature. Aqueous HCl (3 M, 1.4 mL, 4.3 mmol) was added and the mixture was stirred for 10 min followed by the addition of sodium carbonate (0.9 g, 8.6 mmol) and the stirring was continued for another 20 min. 3-Amino-6-bromo-N-(2-morpholin-4-ylethyl)pyrazine-2-carboxamide (0.20 g, 0.61 mmol), and tetrahydrofuran (4 mL) were added followed by addition of Pd(dppf)Cl2 (28 mg, 0.03 mmol) and the resulting mixture was heated at 65° C. for 17 h. The mixture was allowed to return to room temperature and the solvent was evaporated. The resulting residue was suspended in methanol, silica was added, and the solvent was evaporated. Purification by column chromatography on silica using methylene chloride/methanol/triethyl amine, (95:5:0.1), as the eluent gave the free base that was subsequently dissolved in hot methanol and treated with HCl (1 M in diethyl ether). The formed precipitate was filtered off and dried in vacuo to give 72 mg (26% yield) of the title compound as a yellow solid: 1H NMR (DMSO-d6, 400 MHz) δ 11.24 (br s, 1H), 9.28 (m, 1H), 8.98 (s, 1H), 8.49 (d, J=8 Hz, 2H), 7.83 (d, J=8 Hz, 2H), 3.97 (m, 2H), 3.87 (d, J=12 Hz, 2H), 3.78 (m, 2H), 3.55 (d, J=12 Hz, 2H), 3.15 (m, 6H), 1.65 (m, 4H); MS (ES) m/z 461 (M++1).

後処理

  1. temperatureto warm up to room temperature
  2. stirringthe mixture was stirred for 10 min
  3. waitthe stirring was continued for another 20 min
  4. temperaturethe resulting mixture was heated at 65° C. for 17 h
  5. customto return to room temperature
  6. customthe solvent was evaporated
  7. additionsilica was added
  8. customthe solvent was evaporated
  9. customPurification by column chromatography on silica
  10. customgave the free base that
  11. filtrationThe formed precipitate was filtered off
  12. customdried in vacuo

出典と根拠

ORDレコード
ord-f909d4eeb4db48aea4ba57f3131c9267
出典データセット
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07595321B2

反応ノート

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