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Triethylamine → HCID 178462611, 화합물

HRID 267519
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HRID 267519 반응식
[Cl:1][C:2]1[N:11]=[C:10]2[C:5]([C:6](=[O:17])[C:7]([C:14](Cl)=[O:15])=[CH:8][N:9]2[CH2:12][CH3:13])=[CH:4][CH:3]=1.[NH2:18][C:19]1[NH:23][N:22]=[N:21][N:20]=1.C(N(CC)CC)C>O1CCOCC1>[Cl:1][C:2]1[N:11]=[C:10]2[C:5]([C:6](=[O:17])[C:7]([C:14]([NH:18][C:19]3[NH:23][N:22]=[N:21][N:20]=3)=[O:15])=[CH:8][N:9]2[CH2:12][CH3:13])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 21434993HCID 21434993, 화합물HCID 178509299HCID 178509299, 화합물

생성물 1

HCID 178462611HCID 178462611, 화합물

시약·촉매·용매 1

HCID 312751,4-Dioxane용매2회

실험 절차

7-Chloro-1-ethyl-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carbonyl chloride (22.3 g) in dry dioxan (350 ml) was added slowly to 5-amino-1H-tetrazole (7.9 g) and triethylamine (15.1 ml) in dry dioxan (350 ml) and the mixture kept 3 days at room temperature. The solid was collected and dissolved in aqueous dimethylaminoethanol. The solution was filtered and acetic acid was added to the filtrate. The solid that separated was collected and had m.p. above 400°.

후처리

  1. customThe solid was collected
  2. dissolutiondissolved in aqueous dimethylaminoethanol
  3. filtrationThe solution was filtered
  4. additionacetic acid was added to the filtrate
  5. customThe solid that separated
  6. customwas collected

출처 및 근거

ORD 기록
ord-40405b9a7fb844599520380e944f6c0d
출처 데이터셋
uspto-grants-1976_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03943141

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