Glycine methyl ester hydrochloride → HCID 57712377, compound

HRID 2276224Notes

Reaction equation

HRID 2276224 reaction equation
[CH:1]1([C:6]([C:8]2[CH:13]=[C:12]([CH3:14])[CH:11]=[CH:10][C:9]=2[NH:15][C:16]([NH:18][C:19]2[S:20][C:21]([CH:24]=O)=[CH:22][N:23]=2)=[O:17])=[O:7])[CH2:5][CH2:4][CH2:3][CH2:2]1.Cl.[CH3:27][O:28][C:29](=[O:32])[CH2:30][NH2:31]>>[CH3:27][O:28][C:29](=[O:32])[CH2:30][NH:31][CH2:24][C:21]1[S:20][C:19]([NH:18][C:16]([NH:15][C:9]2[CH:10]=[CH:11][C:12]([CH3:14])=[CH:13][C:8]=2[C:6]([CH:1]2[CH2:5][CH2:4][CH2:3][CH2:2]2)=[O:7])=[O:17])=[N:23][CH:22]=1

Participants

3

Reactant 2

HCID 122755Glycine methyl ester hydrochlorideHCID 59733046HCID 59733046, compound

Product 1

HCID 57712377HCID 57712377, compoundYield 45%

Procedure

({2-[3-(2-Cyclopentanecarbonyl-4-methyl-phenyl)-ureido]-thiazol-5-ylmethyl}-amino)-acetic acid methyl ester (38 mg, 45%) was prepared from 1-(2-cyclopentanecarbonyl-4-methyl-phenyl)-3-(5-formyl-thiazol-2-yl)-urea (0.072 g, 0.2 mmol) and glycine methyl ester hydrochloride following the general procedure O.

Sources & evidence

ORD record
ord-06bb5bfddecc47bdb29b731c311c99f7
Source dataset
uspto-grants-2015_09
Patent number
USRE045670E1

Reaction notes

Loading…