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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 58495618, 화합물

HRID 1191025
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HRID 1191025 반응식
C(OC([NH:8][CH2:9][C:10]1[CH:11]=[N:12][C:13]([CH2:16][N:17]2[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]2)=[CH:14][CH:15]=1)=O)(C)(C)C.Cl>CO>[NH2:8][CH2:9][C:10]1[CH:15]=[CH:14][C:13]([CH2:16][N:17]2[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]2)=[N:12][CH:11]=1
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 59828835HCID 59828835, 화합물

생성물 1

HCID 58495618HCID 58495618, 화합물수율 97.1%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
0 °C

실험 절차

Dissolve 3-(tert-butoxycarbonylamino-methyl)-6-(piperidin-1-ylmethyl)-pyridine (540 mg, 1.76 mmol) in methanol (10 mL) and cool to 0° C. Bubble hydrogen chloride through the vigorously stirred solution for 30 min. Concentrate in vacuo. Partition the residue between 3N aqueous NaOH (10 mL) and DCM (20 mL). Separate the two layers and extract the aqueous layer with DCM (2×20 mL). Wash the combined organic extracts with brine (20 mL). Dry over Na2SO4, filter and concentrate in vacuo to obtain the desired intermediate as a colorless oil (351 mg, 95%). MS (APCI+) m/z: 206 (M+H)+.

후처리

  1. concentrationConcentrate in vacuo
  2. customPartition the residue between 3N aqueous NaOH (10 mL) and DCM (20 mL)
  3. customSeparate the two layers
  4. extractionextract the aqueous layer with DCM (2×20 mL)
  5. washWash the combined organic extracts with brine (20 mL)
  6. dry with materialDry over Na2SO4
  7. filtrationfilter
  8. concentrationconcentrate in vacuo

출처 및 근거

ORD 기록
ord-f49713ca9cfc46ab92c26440f18becea
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08680091B2

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