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HCID 19367588,化合物 → 9-Amino-2-(2-fluorophenyl)-7,8,9,10-tetrahydro-imidazo[1,2-c]-quinazolin-5(6H)-one

HRID 22011
笔记
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反应方程式

HRID 22011 反应方程式
C(OC([NH:8][CH:9]1[CH2:18][CH2:17][C:16]2[NH:15][C:14](=[O:19])[N:13]3[CH:20]=[C:21]([C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=4[F:29])[N:22]=[C:12]3[C:11]=2[CH2:10]1)=O)(C)(C)C>FC(F)(F)C(O)=O>[NH2:8][CH:9]1[CH2:18][CH2:17][C:16]2[NH:15][C:14](=[O:19])[N:13]3[CH:20]=[C:21]([C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=4[F:29])[N:22]=[C:12]3[C:11]=2[CH2:10]1
参与物实验过程后处理来源与证据反应笔记

参与物

3

反应物 1

HCID 19367588HCID 19367588,化合物

产物 1

HCID 193675759-Amino-2-(2-fluorophenyl)-7,8,9,10-tetrahydro-imidazo[1,2-c]-quinazolin-5(6H)-one

试剂、催化剂与溶剂 1

HCID 6422三氟乙酸溶剂

实验过程

To 10 mL of trifluoroacetic acid was added 9-(t-Butoxycarbonylamino)-2-(2-fluorophenyl)-7,8,9,10-tetrahydro-imidazo[1,2-c]-quinazolin-5(6H)-one (100 mg). After the solid dissolved, the solution was stirred for 20 minutes and the TFA removed in vacuo. To the residue was added 10 mL of water followed by sufficient saturated aqueous sodium bicarbonate to neutralize the mixture. The mixture was subsequently cooled and the solid collected to yield 9-Amino-2-(2-fluorophenyl)-7,8,9,10-tetrahydro-imidazo[1,2-c]-quinazolin-5(6H)-one (Compound 29), m.p.>325° C.

后处理

  1. dissolutionAfter the solid dissolved
  • customthe TFA removed in vacuo
  • additionTo the residue was added 10 mL of water
  • temperatureThe mixture was subsequently cooled
  • customthe solid collected
  • 来源与证据

    ORD记录
    ord-b2fe13d4988b485d80801c2c0e83ddfd
    来源数据集
    uspto-grants-1995_06
    DOI
    10.6084/m9.figshare.5104873.v1
    专利号
    US05426186

    反应笔记

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    本页导航参与物实验过程后处理来源与证据反应笔记