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HRID339269

反应详情

EQUATION

反应方程式

HRID 339269 的结构方程式

REACTANTS

反应物

2
结构：C[C@@H](C(=O)N[C@H](C(=O)N1Cc2cc(C(=O)O)ccc2C[C@H]1C(=O)N[C@@H]1CCCc2ccccc21)C(C)(C)C)N(C)C(=O)OC(C)(C)C
HCID86705870

未命名化合物

结构：COC(=O)[C@@H]1C[C@H](c2ccc3c(c2)CN(C(=O)[C@@H](NC(=O)[C@H](C)N(C)C(=O)OC(C)(C)C)C(C)(C)C)[C@H](C(=O)N[C@@H]2CCCc4ccccc42)C3)CN1C(=O)[C@@H](NC(=O)[C@H](C)N(C)C(=O)OC(C)(C)C)C(C)(C)C
HCID86705915

未命名化合物

PRODUCTS

生成物

1
结构：C[C@@H](C(=O)N[C@H](C(=O)N1C[C@@H](c2ccc3c(c2)CN(C(=O)[C@@H](NC(=O)[C@H](C)N(C)C(=O)OC(C)(C)C)C(C)(C)C)[C@H](C(=O)N[C@@H]2CCCc4ccccc42)C3)C[C@H]1C(=O)O)C(C)(C)C)N(C)C(=O)OC(C)(C)C
HCID86705914

未命名化合物

收率 95.7%

PROCEDURE

实验过程

Following a procedure analogous to that for the synthesis of Compound K of Example 1, (2S,4R)-methyl 1-((S)-2-((S)-2-((tert-butoxycarbonyl)(methyl)amino)propanamido)-3,3-dimethylbutanoyl)-4-((S)-2-((S)-2-((S)-2-((tert-butoxycarbonyl)(methyl)amino)propanamido)-3,3-dimethylbutanoyl)-3-(((R)-1,2,3,4-tetrahydronaphthalen-1-yl)carbamoyl)-1,2,3,4-tetrahydroisoquinolin-7-yl)pyrrolidine-2-carboxylate (301 mg, 0.29 mmol) was converted to the title compound (282 mg, 95%). MS (ESI+) m/z 1016.7 (M+H)+.