Ethyl 3-(4-aminobenzamido)propanoate → HCID 66777484, compound

HRID 2090920Notes

Reaction equation

HRID 2090920 reaction equation
[CH2:1]([O:8][C:9]1[C:13]([CH:14]([CH:16]2[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]2)O)=[CH:12][N:11]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[N:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:28][C:29]1[CH:34]=[CH:33][C:32]([C:35]([NH:37][CH2:38][CH2:39][C:40]([O:42]CC)=[O:41])=[O:36])=[CH:31][CH:30]=1>>[CH2:1]([O:8][C:9]1[C:13]([CH:14]([NH:28][C:29]2[CH:30]=[CH:31][C:32]([C:35]([NH:37][CH2:38][CH2:39][C:40]([OH:42])=[O:41])=[O:36])=[CH:33][CH:34]=2)[CH:16]2[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]2)=[CH:12][N:11]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[N:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 12469762Ethyl 3-(4-aminobenzamido)propanoateHCID 66777884HCID 66777884, compound

Product 1

HCID 66777484HCID 66777484, compoundYield 43%

Procedure

Using [3-(benzyloxy)-1-phenyl-1H-pyrazol-4-yl](cyclohexyl)methanol (0.79 g) synthesized above and ethyl 3-{[(4-aminophenyl)carbonyl]amino}propanoate (0.51 g) synthesized in Example 1(2) and in the same manner as in Example 1(7), the title object compound (0.51 g, 43%) was obtained as a white solid.

Sources & evidence

ORD record
ord-e392b240f27b49349f9fc86556c7195b
Source dataset
uspto-grants-2013_05
Patent number
US08436043B2

Reaction notes

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