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Hydrochloric Acid → N2-(2,6-Dimethyl-4-pyridyl)propane-1,2-diamine hydrochloride

HRID 333082
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HRID 333082 반응식
[CH3:1][C:2]1[CH:7]=[C:6]([NH:8][CH:9]([CH3:19])[CH2:10][NH:11]C(=O)OC(C)(C)C)[CH:5]=[C:4]([CH3:20])[N:3]=1.[ClH:21]>O1CCOCC1>[ClH:21].[CH3:1][C:2]1[CH:7]=[C:6]([NH:8][CH:9]([CH3:19])[CH2:10][NH2:11])[CH:5]=[C:4]([CH3:20])[N:3]=1
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 86691169Tert-butyl 2-(2,6-dimethylpyridin-4-ylamino)propylcarbamate

생성물 1

HCID 66835507N2-(2,6-Dimethyl-4-pyridyl)propane-1,2-diamine hydrochloride

시약·촉매·용매 1

HCID 312751,4-Dioxane용매2회

실험 절차

To tert-butyl 2-(2,6-dimethylpyridin-4-ylamino)propylcarbamate (147 mg, 0.526 mmol) dissolved in 1,4-dioxane (1 ml) a 4N solution of HCl in dioxane (2 ml, 8.00 mmol) was added. Within a few minutes a precipitate started to form. The solvent was removed in a stream of nitrogen, to the residue was added diethylether and the mixture was allowed to stand at room temperature overnight. The solvent was filtered off, the residue was dried under reduced pressure to yield 135 mg of an off-white solid MS (ESI) m/z=180.0.

후처리

  1. additionwas added
  2. waitWithin a few minutes a precipitate started
  3. customto form
  4. customThe solvent was removed in a stream of nitrogen, to the residue
  5. additionwas added diethylether
  6. filtrationThe solvent was filtered off
  7. customthe residue was dried under reduced pressure

출처 및 근거

ORD 기록
ord-23b3de78bbb24b248281e8b8438fb5c3
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08877934B2

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