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Pyridine → HCID 12521648, 화합물

HRID 436144
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HRID 436144 반응식
[Cl:1][C:2]1[C:17]([Cl:18])=[CH:16][C:5]2[NH:6][C:7](=[O:15])[C:8]3[CH2:14][S:13][CH2:12][C:9]=3[N:10]([CH3:11])[C:4]=2[CH:3]=1.N1C=CC=CC=1.ClN1C(=O)CCC1=O>O>[Cl:1][C:2]1[C:17]([Cl:18])=[CH:16][C:5]2[NH:6][C:7](=[O:15])[C:8]3[C:9](=[CH:12][S:13][CH:14]=3)[N:10]([CH3:11])[C:4]=2[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1049PyridineHCID 31398ChlorosuccinimideHCID 12521637HCID 12521637, 화합물

생성물 1

HCID 12521648HCID 12521648, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a suspension of 0.40 g. of 6,7-dichloro-1,3,4,9-tetrahydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one in 2.7 ml. of dry pyridine is added, in portions. a total of 0.18 g. of N-chlorosuccinimide. The resulting solution is heated on a steam bath for 15 minutes, cooled and diluted with water. The solid which separates is collected and recrystallized from methanol-water to give off-white crystals, m.p. 270°-272° C. (dec.).

후처리

  1. additionTo a suspension of 0.40 g
  2. temperatureThe resulting solution is heated on a steam bath for 15 minutes
  3. temperaturecooled
  4. customThe solid which separates is collected
  5. customrecrystallized from methanol-water
  6. customto give off-white crystals, m.p. 270°-272° C. (dec.)

출처 및 근거

ORD 기록
ord-c51c987e66df4eefadaebd5b7d3d9d99
출처 데이터셋
uspto-grants-1977_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04007272

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