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1,2-Dichloroethane → 1-Methylpyrazol-5-yl 1-Methylbenzotriazole-5-carboxylate

HRID 1263413
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HRID 1263413 반응식
[CH3:1][N:2]1[C:6]2[CH:7]=[CH:8][C:9]([C:11]([OH:13])=[O:12])=[CH:10][C:5]=2[N:4]=[N:3]1.[CH3:14][N:15]1[C:19](O)=[CH:18][CH:17]=[N:16]1.C(#N)C.C(Cl)CCl>CN(C1C=CN=CC=1)C.O.C(N(CC)CC)C>[CH3:1][N:2]1[C:6]2[CH:7]=[CH:8][C:9]([C:11]([O:13][C:19]3[N:15]([CH3:14])[N:16]=[CH:17][CH:18]=3)=[O:12])=[CH:10][C:5]=2[N:4]=[N:3]1
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참가 물질

8

반응물 4

HCID 111,2-DichloroethaneHCID 6342AcetonitrileHCID 27765491-methyl-1H-1,2,3-benzotriazole-5-carboxylic acidHCID 178481816HCID 178481816, 화합물

생성물 1

HCID 186160341-Methylpyrazol-5-yl 1-Methylbenzotriazole-5-carboxylate

시약·촉매·용매 3

HCID 142844-(Dimethylamino)pyridine
촉매
HCID 962Water용매
HCID 8471Triethylamine용매

실험 절차

1.5 g of 1-methylbenzotriazole-5-carboxylic acid (8.5 mmol) and 0.87 g of 1-methyl-5-hydroxypyrazole (8.9 mmol) were dissolved in 70 ml of abs. acetonitrile and admixed with 1.62 g of EDC (8.5 mmol), 2 ml of triethylamine and a catalytic amount of DMAP. After the reaction had ended, the solution was poured into water and the mixture was extracted with ethyl acetate. The organic phase was washed and dried, and the product was then purified by crystallization. Yield: 0.77 g (35%).

후처리

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe organic phase was washed
  3. customdried
  4. customthe product was then purified by crystallization

출처 및 근거

ORD 기록
ord-65c5ee7c7cf14fd28ac87b0307fa786b
출처 데이터셋
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06541423B1

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