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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367907Generated: October 31, 2026

Diisopropylethylamine → N-[7-[(1H-Imidazol-2-ylamino)carbonyl]-1H-benzimidazol-2-yl]thieno[2,3-c]pyridine-5-carboxamide

https://huagongshe.com/reaction/1367907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactantthieno[2,3-c]pyridine-5-carboxylic acid(WXC09021)HCID 12277675—
ReactantHCID 178508178HCID 178508178—
SolventDimethylformamideHCID 6228—
ProductN-[7-[(1H-Imidazol-2-ylamino)carbonyl]-1H-benzimidazol-2-yl]thieno[2,3-c]pyridine-5-carboxamideHCID 587244813%

Reaction Steps

2.6 mg (3%) of thieno[2,3-c]pyridine-5-carboxylic acid [4-(1H-imidazol-2-ylcarbamoyl)-1H-benzoimidazol-2-yl]-amide was prepared according to general procedure A using 54 mg (0.3 mmol) thieno[2,3-c]pyridine-5-carboxylic acid, 61 mg (0.25 mmol) intermediate B (2-amino-3H-benzoimidazole-4-carboxylic acid (1H-imidazol-2-yl)-amide), 114 mg (0.3 mmol) of HBTU, 0.106 mL (0.6 mmol) of DIEA in 1 mL of DMF stirring at 85° C. for 1 h. LCMS: 404 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893267B2
Source datasetuspto-grants-2011_02
ORD IDord-e7b3ed38faad4b69aade29dd8f02db6d
Source noteuspto-grants-2011_02