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【结 构 式】

【分子编号】53102

【品名】tert-butyl 2-{(3R)-3-[4-(3-pyridinyl)-1H-imidazol-1-yl]butyl}-1-hydrazinecarboxylate

【CA登记号】n/a

【 分 子 式 】C17H25N5O2

【 分 子 量 】331.418

【元素组成】C 61.61% H 7.6% N 21.13% O 9.66%

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:(XXVI)

In an alternative synthesis of hydrazine (XXIII), aldehyde (IX) was condensed with tert-butyl hydrazinecarboxylate (XXIV), producing hydrazone (XXV), which was further reduced to the hydrazinecarboxylate (XXVI) in the presence of NaBH(OAc)3. Acidic cleavage of the N-Boc group of (XXVI) provided hydrazine (XXIII).

1 Kaneko, T.; McMillen, W.T.; McLaughlin, R.W.; Ripin, D.H.B.; Vanerplas, B.C. (Pfizer Inc.); Synthesis of carbamate ketolide antibiotics. EP 1088828; JP 2001151792 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IX) 53087 3-[4-(3-pyridinyl)-1H-imidazol-1-yl]butanal n/a C12H13N3O 详情 详情
(XXIII) 53100 3-{1-[(1R)-3-hydrazino-1-methylpropyl]-1H-imidazol-4-yl}pyridine n/a C12H17N5 详情 详情
(XXIV) 10893 tert-butyl 1-hydrazinecarboxylate; tert-butyl carbazate 870-46-2 C5H12N2O2 详情 详情
(XXV) 53101 tert-butyl 2-{(E,3R)-3-[4-(3-pyridinyl)-1H-imidazol-1-yl]butylidene}-1-hydrazinecarboxylate n/a C17H23N5O2 详情 详情
(XXVI) 53102 tert-butyl 2-{(3R)-3-[4-(3-pyridinyl)-1H-imidazol-1-yl]butyl}-1-hydrazinecarboxylate n/a C17H25N5O2 详情 详情
Extended Information