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Hydrochloric Acid → HCID 178507695, 화합물

HRID 2173737
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HRID 2173737 반응식
[H-].[Na+].[C:3](#[N:5])[CH3:4].[N:6]1([CH2:12][C:13](OCC)=O)[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1.O.[NH2:19][NH2:20].Cl>C1(C)C=CC=CC=1.O1CCOCC1>[N:6]1([CH2:12][C:13]2[CH:4]=[C:3]([NH2:5])[NH:20][N:19]=2)[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11]1
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참가 물질

8

반응물 5

HCID 313Hydrochloric Acid2회HCID 6342AcetonitrileHCID 24654Hydrazine hydrate (1:1)HCID 24758Sodium hydrideHCID 6434661-Piperidineacetic acid, ethyl ester

생성물 1

HCID 178507695HCID 178507695, 화합물

시약·촉매·용매 2

HCID 1140
Toluene
용매
2회
HCID 312751,4-Dioxane용매

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온도
80 °C

실험 절차

NaH (0.234 g, 5.84 mmol) in dry toluene (5 ml) was heated to 80° C. A mixture of acetonitrile (0.229 ml, 4.38 mmol), ethyl 1-piperidineacetate (0.5 g, 2.92 mmol) and toluene (3 ml) was added dropwise to the hot reaction mixture. The mixture was stirred at 80° C. for 1.5 hours and after cooling to RT, quenched by the addition of water (6 ml). Hydrazine hydrate (0.142 ml, 2.92 mmol) was added and reaction mixture reheated to 80° C. for 3 hours. The reaction mixture was acidified with 2N HCl (aq.) to pH 2 and loaded onto a SCX-2 cartridge eluting with MeOH followed by 7M NH3 in MeOH. The methanolic ammonia fractions were concentrated in vacuo to afford an oil. 4N HCl in dioxane (15 ml) was added to the yellow oil and the resulting suspension was filtered and washed with iso-hexane to yield the title compound.

후처리

  1. additionwas added dropwise to the hot reaction mixture
  2. temperatureafter cooling to RT
  3. customquenched by the addition of water (6 ml)
  4. customreaction mixture
  5. waitreheated to 80° C. for 3 hours
  6. washeluting with MeOH
  7. concentrationThe methanolic ammonia fractions were concentrated in vacuo
  8. customto afford an oil
  9. filtrationthe resulting suspension was filtered
  10. washwashed with iso-hexane

출처 및 근거

ORD 기록
ord-8bc0a6042efa4edbad0a91f1430644a7
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09056867B2

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