Tetrahydrofuran → (1R,2S)-2-(1H-indazol-6-yl)-5'-methylspiro[cyclopropane-1,3'-indolin]-2'-one

HRID 2383634노트

반응식

HRID 2383634 반응식
C([N:8]1[C:16]2[C:11](=[CH:12][C:13]([CH3:17])=[CH:14][CH:15]=2)[C@:10]2([CH2:19][C@H:18]2[C:20]2[CH:28]=[C:27]3[C:23]([CH:24]=[N:25][N:26]3CC3C=CC=CC=3)=[CH:22][CH:21]=2)[C:9]1=[O:36])C1C=CC=CC=1.C1COCC1.CC([O-])(C)C.[K+]>CS(C)=O>[NH:26]1[C:27]2[C:23](=[CH:22][CH:21]=[C:20]([C@H:18]3[C@@:10]4([C:11]5[C:16](=[CH:15][CH:14]=[C:13]([CH3:17])[CH:12]=5)[NH:8][C:9]4=[O:36])[CH2:19]3)[CH:28]=2)[CH:24]=[N:25]1

참가 물질

5

반응물 3

HCID 8028TetrahydrofuranHCID 23665647Potassium tert-butoxideHCID 67446303(1R,2S)-1'-benzyl-2-(1-benzyl-1H-indazol-6-yl)-5'-methylspiro[cyclopropane-1,3'-indolin]-2'-one2회

생성물 1

HCID 58486155(1R,2S)-2-(1H-indazol-6-yl)-5'-methylspiro[cyclopropane-1,3'-indolin]-2'-one

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

반응 조건

온도
0 °C

실험 절차

To a 100 mL flask charged with (1R,2S)-1′-benzyl-2-(1-benzyl-1H-indazol-6-yl)-5′-methylspiro[cyclopropane-1,3′-indolin]-2′-one (469 mg, 1 mmol) was added dry THF (2 mL) and the resulting mixture was stirred at 0° C. before KOtBu (1 M in THF, 18 mL, 18 mmol) was added over 2 min. After addition, the resulting mixture was stirred for 15 min at 0° C. and DMSO (1.85 mL) was added. Oxygen was bubbled through for 1 h and reaction turned from homogeneous to heterogeneous. LC-MS showed good conversion at 50 min. It was quenched with sat. NH4Cl. The above reaction was repeated on a larger scale using (1R,2S)-1′-benzyl-2-(1-benzyl-1H-indazol-6-yl)-5′-methylspiro[cyclopropane-1,3′-indolin]-2′-one (1.41 g, 3 mmol). After quenching with saturated NH4Cl, two reactions were combined, diluted with H2O and extracted with EtOAc (100 mL×2). Purification by Biotage Isolera (10-95% EtOAc in hexane) gave the title compound as a light solid (680 mg, 53%). 1H NMR (400 MHz, CD3OD) δ 8.02 (s, 1H), 7.67 (d, J=8.4 Hz, 1H), 7.46 (s, 1H), 6.94 (d, J=8.4 Hz, 1H), 6.85 (d, J=8.0 Hz, 1H), 6.81 (d, J=7.6 Hz, 1H), 5.78 (s, 1H), 3.32 (t, overlapping with MeOH residue), 2.20-2.12 (m, 2H), 1.87 (s, 3H); MS ESI 290.1 [M+H]+, calcd for [C18H15N3O+H]+ 290.1.

후처리

  1. additionwas added over 2 min
  2. additionAfter addition
  3. customOxygen was bubbled through for 1 h and reaction
  4. customat 50 min
  5. customIt was quenched with sat. NH4Cl
  6. customThe above reaction
  7. customAfter quenching with saturated NH4Cl, two reactions
  8. additiondiluted with H2O
  9. extractionextracted with EtOAc (100 mL×2)
  10. customPurification by Biotage Isolera (10-95% EtOAc in hexane)

출처 및 근거

ORD 기록
ord-fbbd8ce236c6417ba9c84379ee2a0bb8
출처 데이터셋
uspto-grants-2012_09
특허 번호
US08263596B2

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