Hydrochloric Acid → HCID 69980981, 화합물

HRID 1383773노트

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HRID 1383773 반응식
C(OC([NH:8][C@@H:9]1[CH2:13][CH2:12][N:11]([CH:14]2[CH2:19][CH2:18][C:17]([C:21]3[CH:26]=[CH:25][C:24]([F:27])=[CH:23][CH:22]=3)([OH:20])[CH2:16][CH2:15]2)[CH2:10]1)=O)(C)(C)C.[ClH:28]>C(OCC)(=O)C>[ClH:28].[ClH:28].[NH2:8][C@@H:9]1[CH2:13][CH2:12][N:11]([CH:14]2[CH2:15][CH2:16][C:17]([C:21]3[CH:22]=[CH:23][C:24]([F:27])=[CH:25][CH:26]=3)([OH:20])[CH2:18][CH2:19]2)[CH2:10]1

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 54188068HCID 54188068, 화합물

생성물 1

HCID 69980981HCID 69980981, 화합물수율 89%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

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온도
0 °C

실험 절차

To a solution of 4-((3R)-3-tert-Butoxycarbonylamino-pyrrolidin-1-yl)-1-(4-fluorophenyl) cyclohexanol (1.05 g, 2.8 mmol) in ethyl acetate (50 ml), cooled to 0° C. was added hydrogen chloride gas, bubbled in gently for 5-10 minutes. The reaction mixture was stirred for 20 minutes at 0° C. and the above procedure was repeated twice. Concentration and flushing with ethyl acetate three times gave 4-((3R)-3-aminopyrrolidin-1-yl)-1-(4-fluorophenyl) cyclohexanol dihydrochloride (0.87 g, 89%); 1H NMR (DMSO) δ 11.33 (bd, 1H)), 8.60 (bd, 3H), 7.52 (m, 2H), 7.14 (m,2H), 5.12 (bs, 1H), 3.35-4.04 (m, 6H), 1.76-2.27 (m, 10H).

후처리

  1. custombubbled in gently for 5-10 minutes
  2. concentrationConcentration
  3. customflushing with ethyl acetate three times

출처 및 근거

ORD 기록
ord-ef0bc1de7880448e989dd4a9719caa7e
출처 데이터셋
uspto-grants-2001_07
특허 번호
US06255315B1

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