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Hydrochloric Acid → HCID 18540442, 화합물

HRID 898800
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인쇄 미리보기

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HRID 898800 반응식
[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][CH2:8][CH2:9][CH2:10][N:11]2[CH2:18][CH:17]3[O:19][CH:13]([CH2:14][N:15](C(OC(C)(C)C)=O)[CH2:16]3)[CH2:12]2)=[CH:3][CH:2]=1.Cl>C(OC(=O)C)C>[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][CH2:8][CH2:9][CH2:10][N:11]2[CH2:18][CH:17]3[O:19][CH:13]([CH2:14][NH:15][CH2:16]3)[CH2:12]2)=[CH:3][CH:2]=1
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 18540402HCID 18540402, 화합물

생성물 1

HCID 18540442HCID 18540442, 화합물수율 94%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매2회

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온도
0 °C

실험 절차

tert-Butyl 7-[4-(4-pyridinyl)butyl]-9-oxa-3,7-diazabicyclo[3.3.1]nonane-3-carboxylate (0.9 g, 2.5 mmol, from step (i) above) was dissolved in ethylacetate, and then treated with ethylacetate saturated with HCl at 0° C. The mixture was stirred for 1 h at 0° C., and then at rt overnight. The solvent was evaporated. CH3CN (100 mL) and water (2 mL) were added together with K2CO3 (3.22 g). The mixture was stirred overnight. Filtration and evaporation gave the sub-title compound in 94% yield.

후처리

  1. customat rt
  2. customovernight
  3. customThe solvent was evaporated
  4. additionCH3CN (100 mL) and water (2 mL) were added together with K2CO3 (3.22 g)
  5. stirringThe mixture was stirred overnight
  6. filtrationFiltration and evaporation

출처 및 근거

ORD 기록
ord-d5be74eb9b5c4cdc8f5ba06031af6b30
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07351821B2

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