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HRID1947836

反应详情

EQUATION

反应方程式

HRID 1947836 的结构方程式

REACTANTS

反应物

2
结构：CCOP(=O)(Cc1ccc(Nc2ncc(C(F)(F)F)c(Cl)n2)c(OC)c1)OCC
HCID86654002

未命名化合物

结构：CN1Cc2c(c(N)ccc2[C@H]2CC[C@@H](O)CC2)C1=O
HCID178479966

未命名化合物

PRODUCTS

生成物

1
结构：CCOP(=O)(Cc1ccc(Nc2ncc(C(F)(F)F)c(Nc3ccc([C@H]4CC[C@@H](O)CC4)c4c3C(=O)N(C)C4)n2)c(OC)c1)OCC
HCID178476864

未命名化合物

PROCEDURE

实验过程

This compound was prepared in a manner analogous to Example 87 using diethyl (4-{[4-chloro-5-(trifluoromethyl)pyrimidin-2-yl]amino}-3-methoxybenzyl)phosphonate and 7-amino-4-(cis-4-hydroxycyclohexyl)-2-methyl-2,3-dihydro-1H-isoindol-1-one. Purification: ISCO Combi-flash Rf system, eluting with 0 to 5% MeOH in EtOAc. 1H NMR (400 MHz, DMSO-d6) δ10.56 (s, 1H), 9.00 (s, 1H), 8.37 (s, 1H), 7.47 (br. s., 1H), 7.29 (d, J=8.34 Hz, 1H), 7.06 (s, 1H), 6.91 (d, J=8.08 Hz, 1H), 4.49 (s, 2H), 4.40 (d, J=4.80 Hz, 1H), 3.95-4.07 (m, 4H), 3.91 (br. s., 1H), 3.75 (s, 3H), 3.07 (s, 3H), 1.84-1.97 (m, 2H), 1.77 (d, J=12.38 Hz, 2H), 1.43-1.61 (m, 4H), 1.20 (t, J=6.95 Hz, 6H); MS (ES+): m/z: 678.24 [MH+]. HPLC: tR=3.52 min (ZQ3: polar—5 min).

WORKUP

后处理

  1. customPurification
  2. washISCO Combi-flash Rf system, eluting with 0 to 5% MeOH in EtOAc
  3. customHPLC: tR=3.52 min (ZQ3: polar—5 min)