[7-(2-Tert-butoxycarbonylamino-ethoxy)-2-oxo-1,2,3,4-tetrahydro-quinolin-3-yl]acetic acid methyl ester → [1-Ethyl-7-(4-aminobutoxy)-2-oxo-1,2-dihydro-quinolin-3-yl]acetic Acid Methyl Ester
Reaction equation
COC(=O)CC1CC2C(=CC(OCCNC(OC(C)(C)C)=O)=CC=2)NC1=O.[CH3:28][O:29][C:30](=[O:58])[CH2:31][C:32]1[C:33](=[O:57])[N:34]([CH2:55][CH3:56])[C:35]2[C:40]([CH:41]=1)=[CH:39][CH:38]=[C:37]([O:42][CH2:43][CH2:44][CH2:45][CH2:46][NH:47]C(OC(C)(C)C)=O)[CH:36]=2>>[CH3:28][O:29][C:30](=[O:58])[CH2:31][C:32]1[C:33](=[O:57])[N:34]([CH2:55][CH3:56])[C:35]2[C:40]([CH:41]=1)=[CH:39][CH:38]=[C:37]([O:42][CH2:43][CH2:44][CH2:45][CH2:46][NH2:47])[CH:36]=2Participants
3
Reactant 2
Product 1
Procedure
The title compound is prepared according to the procedure of Example 78 except that [7-(2-tert-butoxycarbonylamino-ethoxy)-2-oxo-1,2,3,4-tetrahydro-quinolin-3-yl]acetic acid methyl ester is replaced with [7-(4-tert-butoxycarbonylaminobutoxy)-1-ethyl-2-oxo-1,2-dihydro-quinolin-3-yl]acetic acid methyl ester.
Sources & evidence
- ORD record
- ord-b122d0e1e90d4b4ca13715cc12578f19
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06429214B1
Reaction notes
Loading…