4-(5-Cyclopropylmethoxy-1,3-benzodioxol-4-yl)-5H-pyrrolo[3,2-d]pyrimidine-7-carboxylic acid → HCID 178496024, compound

HRID 2094181Notes

Reaction equation

HRID 2094181 reaction equation
[CH:1]1([CH2:4][O:5][C:6]2[CH:14]=[CH:13][C:9]3[O:10][CH2:11][O:12][C:8]=3[C:7]=2[C:15]2[C:16]3[NH:23][CH:22]=[C:21]([C:24](O)=[O:25])[C:17]=3[N:18]=[CH:19][N:20]=2)[CH2:3][CH2:2]1.Cl.[CH3:28][O:29][CH2:30][CH2:31][NH:32][C:33]([C@H:35]1[CH2:40][CH2:39][C@H:38]([NH2:41])[CH2:37][CH2:36]1)=[O:34]>>[CH3:28][O:29][CH2:30][CH2:31][NH:32][C:33]([C@H:35]1[CH2:36][CH2:37][C@H:38]([NH:41][C:24]([C:21]2[C:17]3[N:18]=[CH:19][N:20]=[C:15]([C:7]4[C:8]5[O:12][CH2:11][O:10][C:9]=5[CH:13]=[CH:14][C:6]=4[O:5][CH2:4][CH:1]4[CH2:3][CH2:2]4)[C:16]=3[NH:23][CH:22]=2)=[O:25])[CH2:39][CH2:40]1)=[O:34]

Participants

3

Reactant 2

HCID 668660154-(5-Cyclopropylmethoxy-1,3-benzodioxol-4-yl)-5H-pyrrolo[3,2-d]pyrimidine-7-carboxylic acidHCID 178496021HCID 178496021, compound

Product 1

HCID 178496024HCID 178496024, compound

Procedure

Starting from 4-(5-cyclopropylmethoxy-benzo[1,3]dioxol-4-yl)-5H-pyrrolo[3,2-d]pyrimidine-7-carboxylic acid (example A67) and trans-4-amino-cyclohexanecarboxylic acid (2-methoxy-ethyl)-amide hydrochloride (A196) the title compound is obtained as colorless solid.

Sources & evidence

ORD record
ord-a572295d0c8945049fc6d5fa39420bc1
Source dataset
uspto-grants-2013_05
Patent number
US08445501B2

Reaction notes

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