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Chemical Structure| 134784-37-5 Chemical Structure| 134784-37-5

Structure of 134784-37-5

Chemical Structure| 134784-37-5

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Product Details of [ 134784-37-5 ]

CAS No. :134784-37-5
Formula : C5H12N2O3
M.W : 148.16
SMILES Code : O=C(NN)CC(OC)OC

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Application In Synthesis of [ 134784-37-5 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 134784-37-5 ]

[ 134784-37-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 134784-37-5 ]
  • [ 62484-29-1 ]
  • [ 1616707-99-3 ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; at 40℃; for 2h; Step D: N'-(2,8-dichloroquinazolin-4-yl)-3.3-dimethoxypropanehvdrazide [0146] The mixture of <strong>[62484-29-1]2,4,8-trichloroquinazoline</strong> (step C, 4.0 g, 17.2 mmol), DIPEA (15 mL, 86.1 mmol) and 3,3-dimethoxypropanehydrazide (step A, 3.1 g, 20.7 mmol) in 1 ,4- dioxane (50 mL) was stirred at 40 C for 2 hours, and then concentrated. The residue was partitioned between DCM (50 mL) and aqueous NaHC03 (50 mL). The organic layer was washed with water and concentrated to get the title compound as a yellow solid which was characterized by LC/MS. LC-MS: m z (M+l) = 345.
With N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; at 40℃; for 2h; The mixture of <strong>[62484-29-1]2,4,8-trichloroquinazoline</strong> (step C, 4.0 g, 17.2 mmol), DIPEA (15 mL, 86.1 mmol) and 3,3-dimethoxypropanehydrazide (step A, 3.1 g, 20.7 rnrnol) in 1,4-dioxane (50 mL) was stirred at 40C for 2 hours, and then concentrated. The residue was partitioned between DCM (50 rnL) and aqueous NaHCO3 (50 mL). The organic layer was washed with water and concentrated to get the title compound as a yellow solid which was characterized by LC/MS. LC-MS: m/z (M+l) = 345.
With N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; at 40℃; for 2h; The mixture of <strong>[62484-29-1]2,4,8-trichloroquinazoline</strong> (step C, 4.0 g, 17.2 mmol), DIPEA (15 mL, 86.1 mmol) and 3,3-dimethoxypropanehydrazide (step A, 3.1 g, 20.7 mmol) in 1,4-dioxane (50 mL) was stirred at 40C for 2 hours, and then concentrated. The residue was partitioned between DCM (50 mL) and aqueous NaHC( (50 mL). The organic layer was washed with water and concentrated to get the title compound as a yellow solid which was characterized by LC/MS. LC-MS: m/z (M+l) = 345.
 

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