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Sodium hydride → (1S,4R)-4-(3-Cyclohexyl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-ylamine

HRID 572113
ノート
印刷プレビュー

反応式

HRID 572113 の反応式
[NH2:1][C@@H:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C@H:5]([OH:12])[CH2:4][CH2:3]1.[H-].[Na+].[CH:15]1([C:21]2[N:25]3[CH:26]=[C:27](F)[CH:28]=[CH:29][C:24]3=[N:23][N:22]=2)[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1>CN(C=O)C>[CH:15]1([C:21]2[N:25]3[CH:26]=[C:27]([O:12][C@H:5]4[C:6]5[C:11](=[CH:10][CH:9]=[CH:8][CH:7]=5)[C@@H:2]([NH2:1])[CH2:3][CH2:4]4)[CH:28]=[CH:29][C:24]3=[N:23][N:22]=2)[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20]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

5

反応物 3

HCID 24758Sodium hydrideHCID 86686674(1R,4S)-4-Amino-1,2,3,4-tetrahydronaphthalen-1-olHCID 866867283-Cyclohexyl-6-fluoro-[1,2,4]triazolo[4,3-a]pyridine

生成物 1

HCID 86686729(1S,4R)-4-(3-Cyclohexyl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-ylamine

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
60 °C

実験手順

An opaque brown solution of Intermediate 1d (171 mg, 1.05 mmol) and sodium hydride (60% dispersion in oil, 120 mg, 3.00 mmol) in dry DMF (2 mL) was stirred at RT under Argon for 30 min. Intermediate 34b (219 mg, 1.00 mmol) was added, and the resulting dark solution stirred at 60° C. for 2 h. The cooled solution was concentrated in vacuo, redissolved in MeOH (2 mL), applied to an SCX-2 cartridge, and washed with MeOH. The product was eluted with 2M NH3 in MeOH; concentration in vacuo left a brown oil. Flash chromatography (silica 25 g, 2-10% [2M NH3 in MeOH] in DCM) gave a yellow oil. Freeze-drying from MeCN-water (1:2, 3 mL) left the title compound as a pale yellow solid (203 mg, 56%). LCMS (Method 3): Rt 2.29 min, m/z 363 [MH+].

後処理

  1. concentrationThe cooled solution was concentrated in vacuo
  2. dissolutionredissolved in MeOH (2 mL)
  3. washwashed with MeOH
  4. washThe product was eluted with 2M NH3 in MeOH
  5. concentrationconcentration in vacuo
  6. waitleft a brown oil
  7. customFlash chromatography (silica 25 g, 2-10% [2M NH3 in MeOH] in DCM) gave a yellow oil
  8. dry with materialFreeze-drying from MeCN-water (1:2, 3 mL)
  9. waitleft the title compound as a pale yellow solid (203 mg, 56%)

出典と根拠

ORDレコード
ord-c21443b5565849dfa36629c7583e1f46
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09029373B2

反応ノート

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