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HRID455483

反应详情

EQUATION

反应方程式

HRID 455483 的结构方程式

REACTANTS

反应物

3
结构：O=C(O)c1ccc2[nH]c(=O)[nH]c2c1
HCID780757

2-Oxo-2,3-dihydro-1H-benzimidazole-5-carboxylic acid

C8H6N2O3

结构：CN(C)C(On1nnc2cccnc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HCID9886157

Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)

C10H15F6N6OP

结构：c1ccc2c(c1)C[C@@H]1NCCC[C@H]21
HCID58123900

cis-2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridine

C12H15N

PRODUCTS

生成物

1
结构：O=C(c1ccc2[nH]c(=O)[nH]c2c1)N1CCC[C@@H]2c3ccccc3C[C@@H]21
HCID67224616

未命名化合物

收率 11%

PROCEDURE

实验过程

The title compound is prepared from 2-oxo-2,3-dihydro-1H-benzoimidazole-5-carboxylic acid and cis-2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridine following a procedure analogous to that described in Example 1 [2-(7-aza-1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate is used]. Yield: 11% of theory; LC (method 4): tR=1.86 min; Mass spectrum (ESI+): m/z=334 [M+H]+.