Trifluoroacetic acid → (+/-)-trans-N-[(5-methyl-4,5,6,7-tetrahydrothiazolo-[5,4-c]pyridin-2-yl)carbonyl]-1,2-cyclohexanediamine trifluoroacetate

HRID 459468ノート

反応式

HRID 459468 の反応式
C(O[C:6]([NH:8][C@@H:9]1[CH2:14][CH2:13][CH2:12][CH2:11][C@H:10]1[NH2:15])=[O:7])(C)(C)C.[CH3:16][N:17]1[CH2:22][CH2:21][C:20]2[N:23]=[C:24](C([O-])=O)[S:25][C:19]=2[CH2:18]1.[Li+].O.ON1C2C=CC=CC=2N=N1.Cl.CN(C)CCCN=C=NCC.[F:53][C:54]([F:59])([F:58])[C:55]([OH:57])=[O:56]>CN(C)C=O.ClCCl>[F:53][C:54]([F:59])([F:58])[C:55]([OH:57])=[O:56].[CH3:16][N:17]1[CH2:22][CH2:21][C:20]2[N:23]=[C:24]([C:6]([NH:8][C@@H:9]3[CH2:14][CH2:13][CH2:12][CH2:11][C@H:10]3[NH2:15])=[O:7])[S:25][C:19]=2[CH2:18]1

参加物

8

反応物 5

HCID 6422Trifluoroacetic acidHCID 1514390(1R,2R)-trans-N-Boc-1,2-cyclohexanediamineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 27960291-Hydroxybenzotriazole hydrateHCID 23704331Lithium 5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine-2-carboxylate

生成物 1

HCID 18442875(+/-)-trans-N-[(5-methyl-4,5,6,7-tetrahydrothiazolo-[5,4-c]pyridin-2-yl)carbonyl]-1,2-cyclohexanediamine trifluoroacetate

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 6344Dichloromethane溶媒

実験手順

(±)-trans-N-tert-Butoxycarbonyl-1,2-cyclohexane-diamine (642 mg) was dissolved in N,N-dimethylformamide (20 ml), and to the solution lithium 5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine-2-carboxylate (795 mg), 1-hydroxybenzotriazole monohydrate (46 mg) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (2.30 g) were added, and the mixture was stirred overnight at room temperature. After the reaction mixture was concentrated under reduced pressure, and dichloromethane and water were added to the residue, the organic layer was taken out and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by column chromatography on silica gel (dichloromethane:methanol=100:3) to obtain a pale yellow foamy substance. This substance was dissolved in dichloromethane (5 ml), and trifluoroacetic acid (30 ml) was added, and the mixture was stirred at room temperature for 1 minute. The reaction mixture was concentrated under reduced-pressure to obtain the title compound (731 mg) as a pale brown foamy substance.

後処理

  1. concentrationAfter the reaction mixture was concentrated under reduced pressure, and dichloromethane and water
  2. additionwere added to the residue
  3. dry with materialdried over anhydrous sodium sulfate
  4. distillationThe solvent was distilled off under reduced pressure
  5. customthe residue was purified by column chromatography on silica gel (dichloromethane:methanol=100:3)
  6. customto obtain a pale yellow foamy substance
  7. stirringthe mixture was stirred at room temperature for 1 minute
  8. concentrationThe reaction mixture was concentrated under reduced-pressure

出典と根拠

ORDレコード
ord-41142c61bec2417d98cc07b2eff8f53b
出典データセット
uspto-grants-2007_03
特許番号
US07192968B2

反応ノート

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