HCID 86680515, 화합물 → (7R,8aS)-7-Hydroxyhexahydropyrrolo[1,2-a]pyrazin-1(2H)-one

HRID 1184597노트

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HRID 1184597 반응식
[C:1]([CH2:3][N:4]1[CH2:8][C@H:7]([OH:9])[CH2:6][C@H:5]1[C:10]([O:12]C)=O)#[N:2]>[Ni].CO>[OH:9][C@H:7]1[CH2:8][N:4]2[CH2:3][CH2:1][NH:2][C:10](=[O:12])[C@@H:5]2[CH2:6]1

참가 물질

4

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온도
80 °C

실험 절차

(2S,4R)-Methyl 1-(cyanomethyl)-4-hydroxypyrrolidine-2-carboxylate (0.5 g, 2.71 mmol) from Step 1 and methanol (20 mL) were added to Raney®-nickel 2800 water slurry (1.000 g, 17.04 mmol) in a 50 mL pressure bottle. The reaction mixture was stirred for 9 hours under hydrogen (30 psi) at 80° C. The mixture was filtered though a nylon membrane, and the solvent was evaporated in vacuo. The resulting crude oil was purified on a 4 g silica gel cartridge eluted with 20% methanol/dichloromethane over 10 minutes to provide the crude solid product. Further purification on a 4 g cartridge with 20% methanol (2 N ammonia)/dichloromethane afforded (7R,8aS)-7-hydroxy-hexahydropyrrolo[1,2-a]pyrazin-1(2H)-one (0.204 g, 1.303 mmol, 48% yield) as a white solid. 1H NMR (500 MHz, pyridine-d5) δ ppm 8.44 (bs, 1H), 6.57 (d, J=4.0 Hz, 1H), 4.68 (d, J=3.2 Hz, 1H), 3.86 (t, J=8.2 Hz, 1H), 3.54-3.45 (m, 1H), 3.30 (dd, J=10.0, 5.8 Hz, 1H), 3.28-3.23 (m, 1H), 2.95 (dd, J=9.9, 3.6 Hz, 1H), 2.88 (dt, J=12.0, 4.2 Hz, 1H), 2.79 (ddd, J=12.1, 9.4, 4.2 Hz, 1H), 2.61-2.55 (m, 2H); MS (ESI+) m/z 157 (M+H)+.

후처리

  1. filtrationThe mixture was filtered though a nylon membrane
  2. customthe solvent was evaporated in vacuo
  3. customThe resulting crude oil was purified on a 4 g silica gel cartridge
  4. washeluted with 20% methanol/dichloromethane over 10 minutes
  5. customto provide the crude solid product
  6. customFurther purification on a 4 g cartridge with 20% methanol (2 N ammonia)/dichloromethane

출처 및 근거

ORD 기록
ord-2a2d7881df324ddcad22b414ebddb139
출처 데이터셋
uspto-grants-2014_03
특허 번호
US08669255B2

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