Hydrochloric Acid → 2-chloro-7-ethyl-6,7,8,9-tetrahydro-5H-pyrazino[2,3-d]azepine

HRID 408096노트

반응식

HRID 408096 반응식
[CH2:1]([N:3]1[CH2:9][CH2:8][C:7]2[N:10]=[CH:11][C:12](N)=[N:13][C:6]=2[CH2:5][CH2:4]1)[CH3:2].N([O-])=O.[Na+].[ClH:19]>O.[Cu]Br>[Cl:19][C:12]1[CH:11]=[N:10][C:7]2[CH2:8][CH2:9][N:3]([CH2:1][CH3:2])[CH2:4][CH2:5][C:6]=2[N:13]=1

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 30678372-Amino-7-ethyl-6,7,8,9-tetrahydro-5H-pyrazino[2,3-d]azepineHCID 23668193Sodium Nitrite

생성물 1

HCID 580715892-chloro-7-ethyl-6,7,8,9-tetrahydro-5H-pyrazino[2,3-d]azepine

시약·촉매·용매 2

HCID 24593copper(I) bromide촉매HCID 962Water용매

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온도
-5 °C

실험 절차

26.5 g of 7-ethyl-6,7,8,9-tetrahydro-5H-pyrazino[2,3-d]azepin-2-ylamine (U.S. Pat. No. 4,409,220) are suspended in 130 ml conc. hydrochloric acid, combined with 0.1 g copper(I)bromide and cooled to −5° C. A suspension of 11 g sodium nitrite in 14 ml of water is slowly added dropwise. The reaction mixture is stirred for 15 hours at ambient temperature and evaporated almost to dryness. The residue is slowly added to ice water and potassium carbonate. The product is extracted with dichloromethane and precipitated as the hydrochloride with an ethereal HCl solution. 14.3 g product are obtained. M.p.=258-262° C.

후처리

  1. additionis slowly added dropwise
  2. customevaporated almost to dryness
  3. additionThe residue is slowly added to ice water and potassium carbonate
  4. extractionThe product is extracted with dichloromethane
  5. customprecipitated as the hydrochloride with an ethereal HCl solution

출처 및 근거

ORD 기록
ord-9aa18beabcb14f389dd2bab0d4bcbbd9
출처 데이터셋
uspto-grants-2014_06
특허 번호
US08759326B2

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