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Water → 8-chloro-4-(nitrosomethylamino)-1-phenyl-3H-1,5-benzodiazepin-2-one

HRID 1763246
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HRID 1763246 반응식
[N:1]([O-:3])=O.[Na+].[Cl:5][C:6]1[CH:25]=[CH:24][C:9]2[N:10]=[C:11]([NH:22][CH3:23])[CH2:12][C:13](=[O:21])[N:14]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[C:8]=2[CH:7]=1.O>C(O)(=O)C>[Cl:5][C:6]1[CH:25]=[CH:24][C:9]2[N:10]=[C:11]([NH:22][CH2:23][N:1]=[O:3])[CH2:12][C:13](=[O:21])[N:14]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[C:8]=2[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 23668193Sodium NitriteHCID 178482322HCID 178482322, 화합물

생성물 1

HCID 1785263748-chloro-4-(nitrosomethylamino)-1-phenyl-3H-1,5-benzodiazepin-2-one

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

Sodium nitrite, 21.26 g (0.308 m) was added over a period of 20 min to a stirred solution of 71 g (0.237 m) of 7-chloro-3,5-dihydro-2-methylamino-5-phenyl-4H-1,5-benzodiazepin-4-one in 500 ml of acetic acid. Following the addition, the mixture was stirred for 1 hr at room temperature and was then diluted with 1.5 l. of water. The precipitated product was collected, washed with water and dissolved in methylene chloride. The solution was washed with saturated sodium bicarbonate solution, dried over sodium sulfate and evaporated. The residue was crystallized from ether to yield yellow crystals with mp 121°-124°. A second crop was obtained from the mother liquor.

후처리

  1. additionthe addition
  2. additionwas then diluted with 1.5 l
  3. customThe precipitated product was collected
  4. washwashed with water
  5. dissolutiondissolved in methylene chloride
  6. washThe solution was washed with saturated sodium bicarbonate solution
  7. dry with materialdried over sodium sulfate
  8. customevaporated
  9. customThe residue was crystallized from ether
  10. customto yield yellow crystals with mp 121°-124°
  11. customA second crop was obtained from the mother liquor

출처 및 근거

ORD 기록
ord-56c8423a39024ddf94cae43dfdc98012
출처 데이터셋
uspto-grants-1978_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04111931

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