• English
  • 简体中文
Login Register
Current Location: Home > Feedback Help Print

【结 构 式】

【分子编号】56527

【品名】1,6,9,12-tetraoxo-1-phenyl-4-thia-2,7,10,13-tetraazapentadecan-15-oic acid

【CA登记号】

【 分 子 式 】C16H20N4O6S

【 分 子 量 】396.42416

【元素组成】C 48.48% H 5.09% N 14.13% O 24.22% S 8.09%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(XII)

Other S-protecting groups for mercaptoacetyl triglycine have been reported. The S-benzyl derivative (X) was prepared by condensation of triglycine (I) with (benzylthio)acetyl chloride (IX). Alternatively, the S-benzamidomethyl compound (XII) was prepared as follows. Thioglycolic acid (V) was condensed with benzamidomethanol under acidic conditions to give S-(benzamidomethyl)thioglycolic acid (XI), which was then coupled to triglycine (I) using DCC/HOBt. Deprotection in the presence of 99Tc pertechnetate under the same conditions as above furnished the title Tc complex.

1 Okarvi, S.M.; et al.; Comparison of the labelling characteristics of mercaptoacetyltriglycine (MAG3) with different S-protective groups. J Label Compd Radiopharm 1997, 39, 10, 853.
2 Bormans, G.; et al.; Investigation of the labelling characteristics of 99mTc-mercaptoacetyltriglycine. Nucl Med Biol 1995, 22, 3, 339.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 56518 2-({2-[(2-aminoacetyl)amino]acetyl}amino)acetic acid C6H11N3O4 详情 详情
(V) 18524 2-sulfanylacetic acid 68-11-1 C2H4O2S 详情 详情
(IX) 56524 2-(benzylsulfanyl)acetyl chloride C9H9ClOS 详情 详情
(X) 56525 4,7,10-trioxo-1-phenyl-2-thia-5,8,11-triazatridecan-13-oic acid C15H19N3O5S 详情 详情
(XI) 56526 2-{[(benzoylamino)methyl]sulfanyl}acetic acid C10H11NO3S 详情 详情
(XII) 56527 1,6,9,12-tetraoxo-1-phenyl-4-thia-2,7,10,13-tetraazapentadecan-15-oic acid C16H20N4O6S 详情 详情
Extended Information