HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709938Generated: October 27, 2026
Dimethylformamide → 4-Chloro-7H-pyrrolo(2,3-d)pyrimidine-5-carboxamide
https://huagongshe.com/reaction/709938
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4-Chloro-7H-pyrrolo(2,3-d)pyrimidine-5-carboxylic acid | HCID 22460866 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Chloro-7H-pyrrolo(2,3-d)pyrimidine-5-carboxamide | HCID 59361004 | — |
Reaction Steps
To a stirred suspension of 4-chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylic acid (G-1) (3.11 g, 15.7 mmol, 1.0 eq) and a catalytic amount of DMF in a mixture of DCM (40 mL) and THF (40 mL) at RT, oxalyl dichloride (2.0 mL, 23.5 mmol, 1.5 eq) is added dropwise. The resulting mixture is stirred for 2 h and then concentrated in vacuo. The residue (G2) is dissolved in DCM (50 mL) and the resulting solution is added dropwise to saturated aqueous ammonium hydroxide (200 mL) at RT. The resulting mixture is stirred for 30 min and then filtered. The filter cake is then rinsed with H2O (30 mL×2). The filtrate is acidified with con. HCl to adjust the pH to 4-5. The solid is collected by filtration, rinsed with water and dried in vacuo to afford the product, 4-chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carboxamide (G-3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181221B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-5a7238f7a76a43359d758f3ee4f3a9c3 |
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| Source note | uspto-grants-2015_11 |
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